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An Early Feasibility Study Evaluation of an Implant Free Interatrial Shunt to Improve Heart Failure
Sponsor: InterShunt Technologies, Inc.
Summary
The purpose of this early feasibility study is to evaluate the safety and feasibility of the device for percutaneous shunting of the interatrial septum and improvement of heart failure related symptoms. The primary goal is to determine if the device is safe to use. The findings from this study may be used to refine the intended patient population, the design of the device, or develop a subsequent randomized study.
Key Details
Gender
All
Age Range
40 Years - 85 Years
Study Type
INTERVENTIONAL
Enrollment
20
Start Date
2025-05-15
Completion Date
2031-09
Last Updated
2025-09-26
Healthy Volunteers
No
Conditions
Interventions
PAS-C System
All patients will undergo catheterization with the PAS-C System to create an interatrial shunt to reduce left atrial pressure in the heart.
Locations (6)
St. Bernard's Healthcare
Jonesboro, Arkansas, United States
Los Robles Health System
Thousand Oaks, California, United States
Ascension St. Vincent Hospital
Indianapolis, Indiana, United States
Christ Hospital
Cincinnati, Ohio, United States
The Ohio State University
Columbus, Ohio, United States
Methodist Healthcare
San Antonio, Texas, United States