Skip to content

SpyGlass AMEA Registry

Clinical Registry of Cholangioscopy Using the SpyGlass™ Direct Visualization System (DVS) Throughout the AMEA (Asia, Middle-East, Africa) Region

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02281019
Enrollment
526
Registered
2014-11-03
Start date
2014-11-15
Completion date
2016-10-18
Last updated
2019-07-10

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

Conditions

Biliary Obstruction Due to Common Bile Duct Stone, Biliary Stricture, Hemobilia, Periampullary Tumor

Brief summary

The purpose of this study is to document indications for cholangioscopy and clinical utility of the SpyGlass Direct Visualization System (DVS) throughout the AMEA (Asia, Middle-East, Africa) region when used per standard of practice.

Interventions

ERCP procedure will be performed to visualize bile ducts.

DEVICESpyGlass DVS and SpyGlass Digital Simple (DS)

Cholangioscopy using SpyGlass™ DVS or SpyGlass DS will be performed post ERCP for direct viewing of the bile ducts. What is seen during the procedure will determine a course of treatment. Among the options are biopsies taken, stones treated/removed, or a stent placed

Sponsors

Boston Scientific Corporation
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 18 or older. * Willing and able to provide written informed consent to participate in the study. * Willing and able to comply with the study procedures. * Indicated for ERCP and cholangioscopy or indicated for ERCP with suspected need for cholangioscopy.

Exclusion criteria

* Endoscopic techniques are contraindicated. * ERCP is contraindicated * A medical condition that warrants the use of the device outside of the indication for use. * Requirement for anticoagulation that cannot be safely stopped at least 7 days prior to the procedure.

Design outcomes

Primary

MeasureTime frameDescription
Procedural success for indeterminate strictures or undefined filling defectsProcedure - the average expected duration of the procedure is 1.5 hoursFor indeterminate strictures or undefined filling defects cases procedural success is defined as 1) ability to visualize stricture or defect, and 2) ability to provide visual impression of malignancy, and 3) when applicable, ability to obtain SpyBite biopsy adequate for histology
Procedural success for biliary stone casesProcedure - the average expected duration of the procedure is 1.5 hoursFor biliary stone cases procedural success is defined as 1) ability to visualize the stone(s), and 2) ability to successfully initiate stone fragmentation, and 3) ability to achieve stone clearance in one or more SpyGlass procedures.
Procedural success for other indicationsProcedure - the average expected duration of the procedure is 1.5 hoursFor other indications procedural success is defined as ability to establish diagnosis and /or complete therapy in the following categories: 1) pre-operative assessment of extent of peri-ampullary and biliary tumors, 2) selective guidewire placement, 3) assessment of unexplained hemobilia, 4) assessment of portal biliopathy, 5) assessment of intraductal biliary ablation therapy, 6) extraction of migrated stents, or 7) other.

Secondary

MeasureTime frameDescription
Evaluation of serious adverse events (SAEs) related to the SpyGlass devices and/or the SpyGlass procedureProcedure from enrollment through the 72 Hour Post Procedure Follow-up VisitEvaluation of serious adverse events (SAEs) related to the SpyGlass devices and/or the SpyGlass procedure from enrollment through the 72 Hour Post Procedure Follow-up Visit.
Impact of SpyGlass procedure on suspected diagnosis based on prior ERCPProcedure - the average expected duration of the procedure is 1.5 hours
Evaluation of impact of use of antibiotics on incidence of SAEs related to the device and/or procedure.Procedure - the average expected duration of the procedure is 1.5 hours
For patients undergoing SpyBite biopsy: correlation between number of biopsies and conclusive histopathology of SpyBite biopsies.Procedure to 6 monthsAssessment Detail: Endpoint determined for all patients in whom SpyBite biopsy was taken and observed image features were reported. Observed image features include the following categories: None, Growth, Stricture, Hyperplasia, Ulceration, Mass, Dilated tortuous vessels, Papillary or villous projections, Intraductal nodules, Mucus.
For patients undergoing stone management: number of SpyGlass procedures needed to reach stone clearance.Procedure - the average expected duration of the procedure is 1.5 hours
For patients undergoing stone management: correlation between stone size and ability to reach stone clearance in one SpyGlass session.Procedure - the average expected duration of the procedure is 1.5 hours
For patients undergoing stone management: incidence of visualization of stones not suspected during previous ERCP.Procedure - the average expected duration of the procedure is 1.5 hours

Countries

Australia, Hong Kong, India, Japan, Pakistan, Saudi Arabia, Singapore, South Africa, South Korea, Thailand

Outcome results

None listed

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