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RECRUITING
NCT06859970
NA

An Early Feasibility Study Evaluation of an Implant Free Interatrial Shunt to Improve Heart Failure

Sponsor: InterShunt Technologies, Inc.

View on ClinicalTrials.gov

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

Interventions

DEVICE

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