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Study to Evaluate the Safety and Effectiveness of the CODMAN ENTERPRISE® Vascular Reconstruction Device

A Prospective, Multi-center, Single Arm Study to Evaluate the Safety and Effectiveness of the CODMAN ENTERPRISE® Vascular Reconstruction Device and Delivery System When Used in Conjunction With Endovascular Coil Embolization in the Treatment of Wide-necked Saccular Intracranial Aneurysms

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02532517
Enrollment
45
Registered
2015-08-25
Start date
2015-09-01
Completion date
2019-09-21
Last updated
2020-10-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intracranial Aneurysm

Keywords

CODMAN ENTERPRISE® Vascular Reconstruction Device, Wide Neck, Intracranial, Saccular Aneurysms, Cerebral Aneurysms

Brief summary

The purpose of this study is to demonstrate effectiveness and safety of the CODMAN ENTERPRISE® Vascular Reconstruction Device and Delivery System.

Detailed description

The study is a prospective, multi-center, single arm, clinical study to evaluate the safety and effectiveness of the ENTERPRISE stent when used in conjunction with endovascular coil embolization in the treatment of unruptured wide-neck, intracranial, saccular anterior circulation aneurysms (≤ 10 mm). The primary objectives of the study are to evaluate the rate of complete angiographic occlusion at 12 months.

Interventions

DEVICECODMAN ENTERPRISE® Vascular Reconstruction Device and Delivery System

Sponsors

Cerenovus, Part of DePuy Synthes Products, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Target aneurysm is an unruptured wide-neck, intracranial, saccular anterior circulation aneurysm (≤ 10 mm) arising from a parent vessel with a diameter of ≥ 2.5 mm and ≤ 4 mm * Subject understands the nature of the procedure and provides voluntary written informed consent prior to the treatment * Subject is willing to comply with specified follow-up evaluation

Exclusion criteria

* Planned staged procedure * Currently enrolled in another investigational device or drug study * Target aneurysm that has been previously treated * Mycotic, fusiform or dissecting aneurysm * Admission platelet \<50,000 or any known hemorrhagic diathesis, coagulation deficiency, or on oral anticoagulant therapy with an INR \>3.0 * A serum creatinine level \> 2.5 mg/dL within 7 days prior to index procedure

Design outcomes

Primary

MeasureTime frameDescription
Percentage of Participants With Complete Aneurysm Occlusion (RCAO) Without Retreatment at 12-Month Post Procedure12 Months Post ProcedureThe Raymond-Roy Grading scale used for judging intracranial aneurysm (IA) endosaccular embolization success ranges from Grade I to III where, Grade I is completion occlusion with no flow of contrast seen in the aneurysm sac, Grade II is partial occlusion with some flow or eddy flow in the aneurysm sac and Grade III is residual aneurysm or Incomplete occlusion with apparent flow in the aneurysm sac. RCAO was assessed by the Independent Core Laboratory, complete aneurysm occlusion is defined as an aneurysm in which a Grade I (completion occlusion), is achieved on the Raymond Scale at the relevant post-procedure angiogram, without additional procedures for treatment of the aneurysm since the index procedure. Participants who were retreated (retreatment includes staged procedures) prior to the 12-month were considered not to have achieved complete aneurysm occlusion.
Percentage of Participants With Major Ipsilateral Stroke and/or Death Due to Ipsilateral Stroke at 12 Months Post ProcedureAt 12 Months Post ProcedureThe incidence of a major ipsilateral stroke and/or death due to ipsilateral stroke was evaluated from the start of the index procedure until completion of the 12-month follow-up. A major ipsilateral stroke is defined as a new neurological event which is ipsilateral and in the vascular distribution territory of the stenting procedure and that results in an increase of greater than or equal to (\>=) 4 on the National Institute of Health Stroke Scale (NIHSS) as compared to baseline and persists for greater than 24 hours. The NIHSS is a systematic assessment tool that provides a quantitative measure of stroke-related neurologic deficit. The scores range from 0 to 42 with a score of 0 indicates no stroke; 1-4 as minor stroke; 5-15 as moderate stroke; 15-20 as moderate/severe stroke; 21-42 as severe stroke. NIHSS worsening is defined as an increase from baseline of \>= 4.
Percentage of Participant With In-Stent Stenosis at 12 Months Post Procedure Per Independent Core LaboratoryAt 12 Months post procedureIn-stent stenosis is defined as greater than 50 percent (%) narrowing of the vessel within the ENTERPRISE stent or within 10 millimeters (mm) of either end of the stent.

Secondary

MeasureTime frameDescription
Number of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 MonthsImmediately post-procedure (acute), 6 and 12 monthsNumber of Participants with aneurysms occlusion of 100%, 90%-99%, 70-89%, 50-69%, 25-49%, or \<25% occlusion in accordance with Consensus Grades 0 (100% complete aneurysm occlusion) - 5 (\<25% volumetric aneurysm occlusion), respectively, was reported immediately post-procedure (acute), and at the 6 and 12 month follow-up, respectively.
Number of Participants With Aneurysm RecanalizationUp to 12 monthsNumber of participants with aneurysm recanalization was reported. Recanalization was defined as an increase in aneurysm filling as compared to the previous study-specified angiographic assessment, resulting in a change in (that is, worsening of) the Raymond classification.
Number of Participants Retreated With Any Additional TreatmentUp to 12 monthsRetreatment was defined as any additional treatment of the target aneurysm after the index procedure (retreatment includes staged procedures), or an additional procedure (regardless of whether retreatment is by surgery or endovascular treatment) due to recanalization, rupture or bleeding.
Number of Participants With New Neurological Deficits as Per the Modified Rankin Scale (mRS) ScorePost-procedure up to 30-Day, 6-Month Follow-up and 12-Month Follow-upObserved scores on the Modified Ranking Scale was presented at baseline (pre-procedure) and follow-up (30 days, 6 and 12 months post-procedure). mRS score: 0 = no symptoms at all; 1 = no significant disability despite symptoms, able to carry out all usual duties and activities; 2 = slight disability, unable to carry out all previous activities but able to look after own affairs without assistant; 3 = moderate disability, requires some help, but able to walk without assistance; 4 = moderate to severe disability, unable to walk without assistance, and unable to attend own bodily needs without assistance; 5 = severe disability, bedridden, incontinent, and requiring constant nursing care and attention; 6 = dead. The number of participants who had an increase in mRS \> 2 from baseline not related to stroke or death was also be presented for each follow-up time point.
Number of Participants With Procedure Success Immediately Post-procedure (Acute), 6 and 12 MonthsImmediately post-procedure (acute), 6 and 12 monthsThe procedure success rate is defined to be the percentage of aneurysms in which coil mass position is maintained within the sac with parent artery patency, without additional procedures for treatment of the aneurysm since the index procedure. The procedure success was summarized immediately post-treatment (acute), and at the 6- and 12-month follow-up assessments.
Number of Participants With Reduced Thrombolysis in Cerebral Infarction (TICI) Flow (New Occurrence of TICI Grade of 0 or 1)Day 1 (Intraoperative)The percentage of target aneurysms in which a new occurrence of unintentional and persistent reduced TICI flow (TICI grade of 0: No perfusion or 1: Partial perfusion) was observed at the target vessel during the index procedure as a result of a mechanical obstruction such as dissection or luminal thrombus was evaluated. TICI evaluates perfusion severity and ranges from Grade 0 (No perfusion) to 3 (Complete perfusion).
Number of Participants With Bleeding Complications12 monthsThe number of participants who experienced a procedure-related hemorrhagic event which required any of the following was evaluated: blood transfusion, surgical intervention, a new hospitalization, or lengthening of hospital stay. The complications of hematoma requiring treatment (that is, hematoma \> 5 centimeter \[cm\] in diameter occurring at the access site) and retroperitoneal bleeding were reported as hemorrhagic events.
Number of Participants With In-Stent Stenosis Per Independent Core Laboratory During Procedure (Acute), Post-procedure up to 6 Months and 12 Months Follow upDuring procedure (acute), post-procedure up to 6 months and 12 months follow upIn-stent stenosis is defined as greater than 50% narrowing of the vessel within the ENTERPRISE stent or within 10 mm of either end of the stent.
Number of Participants With Thrombosis Per Independent Core LaboratoryDuring procedure (acute), post-procedure up to 6 months and 12 months follow upThrombosis is defined as in-stent thrombosis.
Number of Participants With NIH Stroke Scale (NIHSS) WorseningPost-procedure up to 6-Month and 12-Month Follow-upThe National Institutes of Health Stroke Scale (NIHSS) is a systematic assessment tool that provides a quantitative measure of stroke-related neurologic deficit. The scores range from 0 to 42 with a score of 0 indicates no stroke; 1-4 as minor stroke; 5-15 as moderate stroke; 15-20 as moderate/severe stroke; 21-42 as severe stroke. NIHSS worsening is defined as an increase from baseline of \>= 4.
Number of Participants With Complete Aneurysm Occlusion as Per the Raymond Scale Immediately Post-procedure (Acute), 6 and 12 MonthsImmediately post-procedure (acute), 6 and 12 monthsThe Raymond-Roy Grading scale used for judging intracranial aneurysm (IA) endosaccular embolization success ranges from Grade I to III where, Grade I is completion occlusion with no flow of contrast seen in the aneurysm sac, Grade II is partial occlusion with some flow or eddy flow in the aneurysm sac and Grade III is residual aneurysm or Incomplete occlusion with apparent flow in the aneurysm sac. RCAO was assessed by the Independent Core Laboratory, complete aneurysm occlusion is defined as an aneurysm in which a Grade I (completion occlusion), is achieved on the Raymond Scale at the relevant post-procedure angiogram, without additional procedures for treatment of the aneurysm since the index procedure. Participants who are retreated (retreatment includes staged procedures) prior to the 12-month were considered not to have achieved complete aneurysm occlusion.
Number of Participants With Complete/Partial Aneurysm Occlusion as Per the Raymond Scale Immediately Post-procedure (Acute), 6 and 12 MonthsImmediately post-procedure (acute), 6 and 12 MonthsThe Raymond-Roy Grading scale used for judging intracranial aneurysm (IA) endosaccular embolization success ranges from Grade I to III where, Grade I is completion occlusion with no flow of contrast seen in the aneurysm sac, Grade II is partial occlusion with some flow or eddy flow in the aneurysm sac and Grade III is residual aneurysm or Incomplete occlusion with apparent flow in the aneurysm sac. Complete/partial aneurysm occlusion is defined as an aneurysm in which a score of 1 (complete occlusion) or 2 (residual neck) is achieved on the Raymond Scale, regardless of retreatment. Participants who are retreated (retreatment includes staged procedures) prior to the 12-month post-procedure follow-up visit was considered not to have achieved complete aneurysm occlusion.

Countries

United States

Participant flow

Participants by arm

ArmCount
CODMAN ENTERPRISE
Participants with an unruptured wide-neck, intracranial saccular anterior circulation aneurysm (less than or equal to \[\<=\] 10 millimeters \[mm\]), arising from a parent vessel with a diameter of greater than or equal to \[\>=\] 2.5 mm and \<= 4 mm, treated with either CODMAN ENTERPRISE Vascular Reconstruction Device and Delivery System (ENTERPRISE VRD system) and or CODMAN ENTERPRISE 2 Vascular Reconstruction Device and Delivery System (ENTERPRISE 2 VRD system).
44
Total44

Withdrawals & dropouts

PeriodReasonFG000
Overall StudyDeath4
Overall StudyDid not complete 24-Month visit4
Overall StudyFailed Angiographic eligibility1
Overall StudyLost to Follow-up4
Overall StudyWithdrawal by Subject4

Baseline characteristics

CharacteristicCODMAN ENTERPRISE
Age, Continuous58.4 Years
STANDARD_DEVIATION 12.62
Ethnicity (NIH/OMB)
Hispanic or Latino
5 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
39 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Asian
1 Participants
Race (NIH/OMB)
Black or African American
2 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
3 Participants
Race (NIH/OMB)
White
38 Participants
Sex: Female, Male
Female
30 Participants
Sex: Female, Male
Male
14 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
4 / 44
other
Total, other adverse events
24 / 44
serious
Total, serious adverse events
14 / 44

Outcome results

Primary

Percentage of Participants With Complete Aneurysm Occlusion (RCAO) Without Retreatment at 12-Month Post Procedure

The Raymond-Roy Grading scale used for judging intracranial aneurysm (IA) endosaccular embolization success ranges from Grade I to III where, Grade I is completion occlusion with no flow of contrast seen in the aneurysm sac, Grade II is partial occlusion with some flow or eddy flow in the aneurysm sac and Grade III is residual aneurysm or Incomplete occlusion with apparent flow in the aneurysm sac. RCAO was assessed by the Independent Core Laboratory, complete aneurysm occlusion is defined as an aneurysm in which a Grade I (completion occlusion), is achieved on the Raymond Scale at the relevant post-procedure angiogram, without additional procedures for treatment of the aneurysm since the index procedure. Participants who were retreated (retreatment includes staged procedures) prior to the 12-month were considered not to have achieved complete aneurysm occlusion.

Time frame: 12 Months Post Procedure

Population: Modified Intent to Treat (mITT) analysis set: participants who were found to be eligible for treatment of ENTEPRISE during pre-procedure angiographic assessment, and in whom treatment is attempted. Here 'N' (Number of participants analyzed) included all participants available at 12-month visit with non missing values for this outcome measure (OM).

ArmMeasureValue (NUMBER)
CODMAN ENTERPRISEPercentage of Participants With Complete Aneurysm Occlusion (RCAO) Without Retreatment at 12-Month Post Procedure81.8 Percentage of Participants
Primary

Percentage of Participants With Major Ipsilateral Stroke and/or Death Due to Ipsilateral Stroke at 12 Months Post Procedure

The incidence of a major ipsilateral stroke and/or death due to ipsilateral stroke was evaluated from the start of the index procedure until completion of the 12-month follow-up. A major ipsilateral stroke is defined as a new neurological event which is ipsilateral and in the vascular distribution territory of the stenting procedure and that results in an increase of greater than or equal to (\>=) 4 on the National Institute of Health Stroke Scale (NIHSS) as compared to baseline and persists for greater than 24 hours. The NIHSS is a systematic assessment tool that provides a quantitative measure of stroke-related neurologic deficit. The scores range from 0 to 42 with a score of 0 indicates no stroke; 1-4 as minor stroke; 5-15 as moderate stroke; 15-20 as moderate/severe stroke; 21-42 as severe stroke. NIHSS worsening is defined as an increase from baseline of \>= 4.

Time frame: At 12 Months Post Procedure

Population: mITT analysis set defined as participants who were found to be eligible for treatment of ENTEPRISE during pre-procedure angiographic assessment, and in whom treatment is attempted. Here 'N' (Number of participants analyzed) signifies participants who have been followed-up to the timepoint of interest (12 months) in the population for this OM.

ArmMeasureGroupValue (NUMBER)
CODMAN ENTERPRISEPercentage of Participants With Major Ipsilateral Stroke and/or Death Due to Ipsilateral Stroke at 12 Months Post ProcedureIpsilateral Stroke7.5 Percentage of participants
CODMAN ENTERPRISEPercentage of Participants With Major Ipsilateral Stroke and/or Death Due to Ipsilateral Stroke at 12 Months Post ProcedureDeath related to Ipsilateral Stroke0 Percentage of participants
Primary

Percentage of Participant With In-Stent Stenosis at 12 Months Post Procedure Per Independent Core Laboratory

In-stent stenosis is defined as greater than 50 percent (%) narrowing of the vessel within the ENTERPRISE stent or within 10 millimeters (mm) of either end of the stent.

Time frame: At 12 Months post procedure

Population: mITT analysis set is defined as participants who were found to be eligible for treatment of ENTEPRISE during pre-procedure angiographic assessment, and in whom treatment is attempted. Here 'N' (Number of participants analyzed) signifies all participants who were available at the 12-month visit with non-missing values for this OM.

ArmMeasureValue (NUMBER)
CODMAN ENTERPRISEPercentage of Participant With In-Stent Stenosis at 12 Months Post Procedure Per Independent Core Laboratory0.0 Percentage of participants
Secondary

Number of Participants Retreated With Any Additional Treatment

Retreatment was defined as any additional treatment of the target aneurysm after the index procedure (retreatment includes staged procedures), or an additional procedure (regardless of whether retreatment is by surgery or endovascular treatment) due to recanalization, rupture or bleeding.

Time frame: Up to 12 months

Population: mITT analysis set: participants who were found to be eligible for treatment of ENTEPRISE during pre-procedure angiographic assessment, and in whom treatment is attempted. Here 'N' (number of participants analyzed) included participants who had been followed up to 12-month follow-up, or otherwise who were retreated prior to 12-Month Follow-up.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
CODMAN ENTERPRISENumber of Participants Retreated With Any Additional Treatment0 Participants
Secondary

Number of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 Months

Number of Participants with aneurysms occlusion of 100%, 90%-99%, 70-89%, 50-69%, 25-49%, or \<25% occlusion in accordance with Consensus Grades 0 (100% complete aneurysm occlusion) - 5 (\<25% volumetric aneurysm occlusion), respectively, was reported immediately post-procedure (acute), and at the 6 and 12 month follow-up, respectively.

Time frame: Immediately post-procedure (acute), 6 and 12 months

Population: mITT analysis set included. Here 'N' (Number of participants analyzed) signifies all evaluable participants with valid assessments post procedure for this OM and 'n' (number analyzed) signifies number of participants available at the specified visits with non-missing values of the OM.

ArmMeasureGroupCategoryValue (COUNT_OF_PARTICIPANTS)
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 MonthsImmediately post-procedure (acute)100%16 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 MonthsImmediately post-procedure (acute)90% - 99%26 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 MonthsImmediately post-procedure (acute)70% - 89%0 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 MonthsImmediately post-procedure (acute)50% - 69%0 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 MonthsImmediately post-procedure (acute)25% - 49%0 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 MonthsImmediately post-procedure (acute)<25%0 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 Months6-Month Follow-up100%24 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 Months6-Month Follow-up90% - 99%8 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 Months6-Month Follow-up70% - 89%2 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 Months6-Month Follow-up50% - 69%0 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 Months6-Month Follow-up25% - 49%0 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 Months6-Month Follow-up<25%0 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 Months12-Month Follow-up100%18 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 Months12-Month Follow-up90% - 99%3 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 Months12-Month Follow-up70% - 89%1 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 Months12-Month Follow-up50% - 69%0 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 Months12-Month Follow-up25% - 49%0 Participants
CODMAN ENTERPRISENumber of Participants With 25% to 100% Aneurysm Occlusion Immediately Post-procedure (Acute), 6 and 12 Months12-Month Follow-up<25%0 Participants
Secondary

Number of Participants With Aneurysm Recanalization

Number of participants with aneurysm recanalization was reported. Recanalization was defined as an increase in aneurysm filling as compared to the previous study-specified angiographic assessment, resulting in a change in (that is, worsening of) the Raymond classification.

Time frame: Up to 12 months

Population: mITT analysis set is defined as participants who were found to be eligible for treatment of ENTEPRISE during pre-procedure angiographic assessment, and in whom treatment is attempted. Here 'N' (number of participants analyzed) included all evaluable participants with data available for this OM.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
CODMAN ENTERPRISENumber of Participants With Aneurysm Recanalization2 Participants
Secondary

Number of Participants With Bleeding Complications

The number of participants who experienced a procedure-related hemorrhagic event which required any of the following was evaluated: blood transfusion, surgical intervention, a new hospitalization, or lengthening of hospital stay. The complications of hematoma requiring treatment (that is, hematoma \> 5 centimeter \[cm\] in diameter occurring at the access site) and retroperitoneal bleeding were reported as hemorrhagic events.

Time frame: 12 months

Population: mITT analysis set included. Here 'N' (Number of participants analyzed) included all participants with data available for this OM and 'n' (number analyzed) signifies number of participants analyzed at specified time points.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
CODMAN ENTERPRISENumber of Participants With Bleeding ComplicationsPost-procedure up to 6-Month Follow-up3 Participants
CODMAN ENTERPRISENumber of Participants With Bleeding ComplicationsPost-procedure up to 12-Month Follow-up3 Participants
Secondary

Number of Participants With Complete Aneurysm Occlusion as Per the Raymond Scale Immediately Post-procedure (Acute), 6 and 12 Months

The Raymond-Roy Grading scale used for judging intracranial aneurysm (IA) endosaccular embolization success ranges from Grade I to III where, Grade I is completion occlusion with no flow of contrast seen in the aneurysm sac, Grade II is partial occlusion with some flow or eddy flow in the aneurysm sac and Grade III is residual aneurysm or Incomplete occlusion with apparent flow in the aneurysm sac. RCAO was assessed by the Independent Core Laboratory, complete aneurysm occlusion is defined as an aneurysm in which a Grade I (completion occlusion), is achieved on the Raymond Scale at the relevant post-procedure angiogram, without additional procedures for treatment of the aneurysm since the index procedure. Participants who are retreated (retreatment includes staged procedures) prior to the 12-month were considered not to have achieved complete aneurysm occlusion.

Time frame: Immediately post-procedure (acute), 6 and 12 months

Population: mITT analysis set included. Here 'N' (Number of participants analyzed) signifies all evaluable participants with valid assessments post procedure for this OM and 'n' (number analyzed) signifies participants available at the schedule visits with non-missing values of the OM.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
CODMAN ENTERPRISENumber of Participants With Complete Aneurysm Occlusion as Per the Raymond Scale Immediately Post-procedure (Acute), 6 and 12 MonthsImmediately post-procedure (acute)16 Participants
CODMAN ENTERPRISENumber of Participants With Complete Aneurysm Occlusion as Per the Raymond Scale Immediately Post-procedure (Acute), 6 and 12 Months6-Month Follow Up24 Participants
CODMAN ENTERPRISENumber of Participants With Complete Aneurysm Occlusion as Per the Raymond Scale Immediately Post-procedure (Acute), 6 and 12 Months12-Month Follow Up18 Participants
Secondary

Number of Participants With Complete/Partial Aneurysm Occlusion as Per the Raymond Scale Immediately Post-procedure (Acute), 6 and 12 Months

The Raymond-Roy Grading scale used for judging intracranial aneurysm (IA) endosaccular embolization success ranges from Grade I to III where, Grade I is completion occlusion with no flow of contrast seen in the aneurysm sac, Grade II is partial occlusion with some flow or eddy flow in the aneurysm sac and Grade III is residual aneurysm or Incomplete occlusion with apparent flow in the aneurysm sac. Complete/partial aneurysm occlusion is defined as an aneurysm in which a score of 1 (complete occlusion) or 2 (residual neck) is achieved on the Raymond Scale, regardless of retreatment. Participants who are retreated (retreatment includes staged procedures) prior to the 12-month post-procedure follow-up visit was considered not to have achieved complete aneurysm occlusion.

Time frame: Immediately post-procedure (acute), 6 and 12 Months

Population: mITT analysis set included. Here 'N' (Number of participants analyzed) signifies all evaluable participants with valid assessments post procedure for this OM and 'n' (number analyzed) signifies number of participants available at the specified visits with non-missing values of the OM.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
CODMAN ENTERPRISENumber of Participants With Complete/Partial Aneurysm Occlusion as Per the Raymond Scale Immediately Post-procedure (Acute), 6 and 12 MonthsImmediately post-procedure (acute)34 Participants
CODMAN ENTERPRISENumber of Participants With Complete/Partial Aneurysm Occlusion as Per the Raymond Scale Immediately Post-procedure (Acute), 6 and 12 Months6-Month Follow Up32 Participants
CODMAN ENTERPRISENumber of Participants With Complete/Partial Aneurysm Occlusion as Per the Raymond Scale Immediately Post-procedure (Acute), 6 and 12 Months12-Month Follow Up21 Participants
Secondary

Number of Participants With In-Stent Stenosis Per Independent Core Laboratory During Procedure (Acute), Post-procedure up to 6 Months and 12 Months Follow up

In-stent stenosis is defined as greater than 50% narrowing of the vessel within the ENTERPRISE stent or within 10 mm of either end of the stent.

Time frame: During procedure (acute), post-procedure up to 6 months and 12 months follow up

Population: mITT analysis set included. Here 'N' (Number of participants analyzed) included all participants with data available for this OM and 'n' (number analyzed) signifies number of participants analyzed at specified time points.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
CODMAN ENTERPRISENumber of Participants With In-Stent Stenosis Per Independent Core Laboratory During Procedure (Acute), Post-procedure up to 6 Months and 12 Months Follow upDuring procedure (acute)0 Participants
CODMAN ENTERPRISENumber of Participants With In-Stent Stenosis Per Independent Core Laboratory During Procedure (Acute), Post-procedure up to 6 Months and 12 Months Follow upPost-procedure up to 6-Month Follow-up0 Participants
CODMAN ENTERPRISENumber of Participants With In-Stent Stenosis Per Independent Core Laboratory During Procedure (Acute), Post-procedure up to 6 Months and 12 Months Follow upPost-procedure up to 12-Month Follow-up0 Participants
Secondary

Number of Participants With New Neurological Deficits as Per the Modified Rankin Scale (mRS) Score

Observed scores on the Modified Ranking Scale was presented at baseline (pre-procedure) and follow-up (30 days, 6 and 12 months post-procedure). mRS score: 0 = no symptoms at all; 1 = no significant disability despite symptoms, able to carry out all usual duties and activities; 2 = slight disability, unable to carry out all previous activities but able to look after own affairs without assistant; 3 = moderate disability, requires some help, but able to walk without assistance; 4 = moderate to severe disability, unable to walk without assistance, and unable to attend own bodily needs without assistance; 5 = severe disability, bedridden, incontinent, and requiring constant nursing care and attention; 6 = dead. The number of participants who had an increase in mRS \> 2 from baseline not related to stroke or death was also be presented for each follow-up time point.

Time frame: Post-procedure up to 30-Day, 6-Month Follow-up and 12-Month Follow-up

Population: mITT analysis set: participants who were found to be eligible for treatment of ENTEPRISE during pre-procedure angiographic assessment, and in whom treatment is attempted. Here 'n' (number analyzed) signifies number of participants available at the specified visits with non-missing values of the OM.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
CODMAN ENTERPRISENumber of Participants With New Neurological Deficits as Per the Modified Rankin Scale (mRS) ScorePost-procedure up to 30-Day Follow-up5 Participants
CODMAN ENTERPRISENumber of Participants With New Neurological Deficits as Per the Modified Rankin Scale (mRS) ScorePost-procedure up to 6-Month Follow-up5 Participants
CODMAN ENTERPRISENumber of Participants With New Neurological Deficits as Per the Modified Rankin Scale (mRS) ScorePost-procedure up to 12-Month Follow-up5 Participants
Secondary

Number of Participants With NIH Stroke Scale (NIHSS) Worsening

The National Institutes of Health Stroke Scale (NIHSS) is a systematic assessment tool that provides a quantitative measure of stroke-related neurologic deficit. The scores range from 0 to 42 with a score of 0 indicates no stroke; 1-4 as minor stroke; 5-15 as moderate stroke; 15-20 as moderate/severe stroke; 21-42 as severe stroke. NIHSS worsening is defined as an increase from baseline of \>= 4.

Time frame: Post-procedure up to 6-Month and 12-Month Follow-up

Population: mITT analysis set included. Here 'N' (Number of participants analyzed) included participants who had at least one post-baseline NIHSS scores and 'n' (number analyzed) signifies number of participants analyzed at specified time points.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
CODMAN ENTERPRISENumber of Participants With NIH Stroke Scale (NIHSS) WorseningPost-procedure up to 6-Month Follow-up2 Participants
CODMAN ENTERPRISENumber of Participants With NIH Stroke Scale (NIHSS) WorseningPost-procedure up to 12-Month Follow-up2 Participants
Secondary

Number of Participants With Procedure Success Immediately Post-procedure (Acute), 6 and 12 Months

The procedure success rate is defined to be the percentage of aneurysms in which coil mass position is maintained within the sac with parent artery patency, without additional procedures for treatment of the aneurysm since the index procedure. The procedure success was summarized immediately post-treatment (acute), and at the 6- and 12-month follow-up assessments.

Time frame: Immediately post-procedure (acute), 6 and 12 months

Population: mITT analysis set is defined as participants who were found to be eligible for treatment of ENTEPRISE during pre-procedure angiographic assessment, and in whom treatment is attempted. Here 'n' (number analyzed) signifies participants available at specified visits with non-missing values of the OM.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
CODMAN ENTERPRISENumber of Participants With Procedure Success Immediately Post-procedure (Acute), 6 and 12 MonthsImmediately post-procedure (acute)41 Participants
CODMAN ENTERPRISENumber of Participants With Procedure Success Immediately Post-procedure (Acute), 6 and 12 Months6-Month Follow-up34 Participants
CODMAN ENTERPRISENumber of Participants With Procedure Success Immediately Post-procedure (Acute), 6 and 12 Months12-Month Follow-up23 Participants
Secondary

Number of Participants With Reduced Thrombolysis in Cerebral Infarction (TICI) Flow (New Occurrence of TICI Grade of 0 or 1)

The percentage of target aneurysms in which a new occurrence of unintentional and persistent reduced TICI flow (TICI grade of 0: No perfusion or 1: Partial perfusion) was observed at the target vessel during the index procedure as a result of a mechanical obstruction such as dissection or luminal thrombus was evaluated. TICI evaluates perfusion severity and ranges from Grade 0 (No perfusion) to 3 (Complete perfusion).

Time frame: Day 1 (Intraoperative)

Population: mITT analysis set is defined as participants who were found to be eligible for treatment of ENTEPRISE during pre-procedure angiographic assessment, and in whom treatment is attempted.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
CODMAN ENTERPRISENumber of Participants With Reduced Thrombolysis in Cerebral Infarction (TICI) Flow (New Occurrence of TICI Grade of 0 or 1)2 Participants
Secondary

Number of Participants With Thrombosis Per Independent Core Laboratory

Thrombosis is defined as in-stent thrombosis.

Time frame: During procedure (acute), post-procedure up to 6 months and 12 months follow up

Population: mITT analysis set included. Here 'N' (Number of participants analyzed) included all participants with data available for this OM and 'n' (number analyzed) signifies number of participants analyzed at specified time points.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
CODMAN ENTERPRISENumber of Participants With Thrombosis Per Independent Core LaboratoryDuring procedure (acute)1 Participants
CODMAN ENTERPRISENumber of Participants With Thrombosis Per Independent Core LaboratoryPost-procedure up to 6-Month Follow-up0 Participants
CODMAN ENTERPRISENumber of Participants With Thrombosis Per Independent Core LaboratoryPost-procedure up to 12-Month Follow-up0 Participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026