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NHLBI SESAME (SEptal Scoring Along Midline Endocardium) Early Feasibility Study

NHLBI SESAME (SEptal Scoring Along Midline Endocardium) Early Feasibility Study

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06269640
Enrollment
1
Registered
2024-02-21
Start date
2024-12-18
Completion date
2024-12-23
Last updated
2025-12-18

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

Conditions

Aortic Valve Stenosis, Hypertrophic Cardiomyopathy, Left Ventricular Septal Hypertrophy, Mitral Valve Disease

Keywords

transcatheter electrosurgery, transcatheter ventricular myotomy, Cardiac interventricular septal reduction

Brief summary

Background: Some people have a condition in which the wall (septum) that separates the two main pumping chambers of the heart is too thick. This thick septum causes a condition called left ventricular outflow tract obstruction (LVOTO), which reduces blood flow out of the heart. LVOTO can cause serious heart disease; symptoms may include shortness of breath, chest pain, heart failure, or death. Researchers want to find better ways to treat LVOTO. Objective: To test a new procedure where excess tissue is sliced away from the septum in people with LVOTO. This procedure is called septal scoring along midline endocardium (SESAME). Eligibility: Adults aged 21 years with LVOTO. Design: Participants will have baseline tests. They will have imaging scans and tests of their heart structure and function. They will take a walking test and answer questions about how their heart condition affects their life. Participants will stay in the hospital 2 to 6 days for the SESAME procedure. They will be completely or partially asleep for the procedure. A tube will be inserted into the mouth and down the throat to take pictures of the heart. Pictures may also be taken with a tube inserted inside the heart. Next, tubes will be inserted into the groin and guided through the blood vessels up to the heart. Guidewires will be inserted into the heart. Doctors will watch the path the wires take with x-rays and ultrasound. When the wire is in the correct place, it will be electrified to slice excess tissue away from the septum. Participants will have 3 follow-up visits within 1 year.

Detailed description

Cardiac interventricular septal reduction therapies - to relieve left ventricular outflow tract obstruction from transcatheter valve replacement or hypertrophic cardiomyopathy - have inherent limitations including dependence on coronary anatomy, high pacemaker implantation rate, and surgical morbidity. We developed a novel transcatheter ventricular myotomy called SEptal Scoring Along the Midline Endocardium (SESAME) that relies on intramyocardial guidewire navigation and transcatheter electrosurgery. SESAME has been performed on a small number of patients using off label devices. This study systematically characterizes the safety and early feasibility of SESAME at 2 enrolling site. SESAME is performed as septal reduction therapy in a heterogeneous group of subjects, including symptomatic hypertrophic cardiomyopathy and resting or provoked left ventricular outflow obstruction (LVOTO); and severe symptomatic mitral and/or aortic valve disease at high risk of standard heart surgical therapy and requiring later transcatheter heart valve implantation combined with manifest or potential LVOTO. A key goal of this study is to attempt to capture generalizable knowledge from as many patients as possible, and to add a limited number of research procedures to characterize the safety and provisional effectiveness of SESAME. Absent realistic non-clinical models of HCM or LVH combined with aortomitral disease, we believe little more information can be gleaned without clinical investigation. This protocol was revised to add a second enrolling medical center, and to focus inclusion criteria on research participants with hypertrophic cardiomyopathy (HCM). This protocol was further revised after the first subject died as a result of excessively-deep SESAME laceration. The required septal thickness for eligibility was increased from \>=12mm to \>=16mm.

Interventions

DEVICESeptal Scoring Along Midline Endocardium

Transcatheter ventricular myotomy called SEptal Scoring Along the Midline Endocardium (SESAME) that relies on intramyocardial guidewire navigation and transcatheter electrosurgery

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
Lead SponsorNIH

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* INCLUSION CRITERIA: * Adults age \>= 21 years * Requires debulking of left ventricular septum for hypertrophic cardiomyopathy * Septal diastolic thickness of obstructive hump on CT: * Total \>=16 mm, and * Predicted residual septal thickness \>= 8 mm, and * Predicted laceration depth \>= 6 mm * Severely symptomatic, any of * NYHA Class III or greater * Canadian Angina Class CCS III or greater * Explicitly chooses investigational SESAME over conventional treatment approaches including (1) cardiac myosin inhibitor therapy, if eligible; (2) transcoronary alcohol septal ablation, if eligible; or (3) surgical left ventricular myotomy and/or myectomy, if eligible * Concurrence of the multidisciplinary institutional heart team that the candidate is at high risk for surgical myectomy * Concurrence of the study Central Clinical Eligibility Committee * Willing to return for all scheduled follow-up activities, and eligible or able to undergo required protocol and testing

Exclusion criteria

* Does not consent to participate, or unable to consent to participate * Requires antegrade SESAME access (because of mechanical aortic valve) * Prior completed transcoronary alcohol septal ablation, or prior surgical myectomy * Pregnant * Hemodynamic instability or emergency procedure * eGFR \< 30 mL/min/1.73m\^2 * Survival despite successful procedure expected \< 12months

Design outcomes

Primary

MeasureTime frameDescription
Number of Participant That Experienced Technical Success With the SESAME (SEptal Scoring Along Midline Endocardium)1 minute following procedure discharge (Exit from the catheterization laboratory)The primary feasibility endpoint is Technical success with the SESAME (SEptal Scoring Along Midline Endocardium) technique. All of the following must be present: * Alive * Procedure success including * Successful myocardial entry, navigation, and snaring of guidewire traversal system; and * Successful laceration of septal myocardium
Number of Inpatient Safety Events Related to SESAME (SEptal Scoring Along Midline Endocardium)Up to 4 daysNumber of Inpatient Safety Events related to SESAME (SEptal Scoring Along Midline Endocardium) Safety is measured as freedom from all of the following: * All-cause mortality * All stroke (disabling and non-disabling) * Major cardiac structural complication requiring intervention (such as iatrogenic ventricular septal defect, iatrogenic aortic valve regurgitation, iatrogenic mitral regurgitation, or pericardial tamponade).

Secondary

MeasureTime frameDescription
Number of Complete Heart Block EventsUp to 4 DaysNumber of Complete heart block events requiring permanent pacemaker included in cardiac arrest

Countries

United States

Participant flow

Participants by arm

ArmCount
Participants Undergoing SEptal Scoring Along Midline Endocardium (SESAME) Procedure
Participants Undergoing SEptal Scoring Along Midline Endocardium (SESAME) Procedure that relies on intramyocardial guidewire navigation and transcatheter electrosurgery.
1
Total1

Withdrawals & dropouts

PeriodReasonFG000
Overall StudyDeath1

Baseline characteristics

CharacteristicParticipants Undergoing SEptal Scoring Along Midline Endocardium (SESAME) Procedure
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
1 Participants
Age, Categorical
Between 18 and 65 years
0 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
1 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Asian
0 Participants
Race (NIH/OMB)
Black or African American
0 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
0 Participants
Race (NIH/OMB)
White
1 Participants
Region of Enrollment
United States
1 participants
Sex: Female, Male
Female
1 Participants
Sex: Female, Male
Male
0 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
1 / 1
other
Total, other adverse events
0 / 1
serious
Total, serious adverse events
1 / 1

Outcome results

Primary

Number of Inpatient Safety Events Related to SESAME (SEptal Scoring Along Midline Endocardium)

Number of Inpatient Safety Events related to SESAME (SEptal Scoring Along Midline Endocardium) Safety is measured as freedom from all of the following: * All-cause mortality * All stroke (disabling and non-disabling) * Major cardiac structural complication requiring intervention (such as iatrogenic ventricular septal defect, iatrogenic aortic valve regurgitation, iatrogenic mitral regurgitation, or pericardial tamponade).

Time frame: Up to 4 days

ArmMeasureValue (NUMBER)
Participants Undergoing SEptal Scoring Along Midline Endocardium (SESAME) ProcedureNumber of Inpatient Safety Events Related to SESAME (SEptal Scoring Along Midline Endocardium)2 Number of Safety Events
Primary

Number of Participant That Experienced Technical Success With the SESAME (SEptal Scoring Along Midline Endocardium)

The primary feasibility endpoint is Technical success with the SESAME (SEptal Scoring Along Midline Endocardium) technique. All of the following must be present: * Alive * Procedure success including * Successful myocardial entry, navigation, and snaring of guidewire traversal system; and * Successful laceration of septal myocardium

Time frame: 1 minute following procedure discharge (Exit from the catheterization laboratory)

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Participants Undergoing SEptal Scoring Along Midline Endocardium (SESAME) ProcedureNumber of Participant That Experienced Technical Success With the SESAME (SEptal Scoring Along Midline Endocardium)1 Participants
Secondary

Number of Complete Heart Block Events

Number of Complete heart block events requiring permanent pacemaker included in cardiac arrest

Time frame: Up to 4 Days

ArmMeasureValue (NUMBER)
Participants Undergoing SEptal Scoring Along Midline Endocardium (SESAME) ProcedureNumber of Complete Heart Block Events1 Complete Heart Block Events

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