Clinical Trial

Initial Study of a MOTHER-DAUGHTER SIDE-BRANCH ACCESS™ DES System (FIH Feasibility Study)

Name: Initial Study of a MOTHER-DAUGHTER SIDE-BRANCH ACCESS™ DES System (FIH Feasibility Study) — clinical trial record (NCT07649798)
Creator: DataLookout
License: https://creativecommons.org/licenses/by/4.0/

Active, Not Recruiting

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Summary

This first in human feasibility study is designed to evaluate the feasibility MD-SBA DES in subjects undergoing percutaneous coronary intervention (PCI) to treat bifurcation lesions.

Protocol Amendment History 1 amendment

This ClinicalTrials.gov record has been amended once since 2026-06-11.

Trial Details

NCT Number	NCT07649798
Lead Sponsor	Advanced Bifurcation Systems Inc.
Conditions	Coronary Angioplasty, Bifurcation Coronary Artery Disease, Ischemic Heart Disease (IHD), Percutaneous Coronary Intervention (PCI)
Enrollment	13 participants
Start Date	2025-09-16
Primary Completion	2025-11-19 (estimated)
Study Completion	2028-11-19 (estimated)
Updated on ClinicalTrials.gov	2026-06-29