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Completed Not applicable Interventional Results available

C-Pulse IDE Feasibility Study- A Heart Assist System

ClinicalTrials.gov ID: NCT00815880

Public ClinicalTrials.gov record NCT00815880. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 4, 2026, 3:58 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

C-Pulse Implantable Counterpulsation Pump (ICP) Feasibility Study - A Heart Assist System

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The C-Pulse Feasibility Study is evaluating the safety and performance of a new product for the treatment of heart failure. The product is designed to help reduce the symptoms of heart failure and help patients function better with daily activities. The study evaluates multiple measures of heart function and whether the patient's quality of life has been improved since the device implant. The patient will have several visits after the device implant to assess how well they are doing and to monitor any safety concerns.

Study identification

NCT ID
NCT00815880
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Nuwellis, Inc.
Industry
Enrollment
21 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 9, 2008
Primary completion
May 6, 2018
Completion
Sep 6, 2018
Last update posted
Aug 23, 2023

2008 – 2018

United States locations

U.S. sites
6
U.S. states
6
U.S. cities
6
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294
University of Louisville Louisville Kentucky 40202
St. Paul Heart Clinic Saint Paul Minnesota 55102
Mid America Heart Institute-Saint Luke's Hospital Kansas City Missouri 64111
Ohio State University Columbus Ohio 43210
Penn State Milton S. Hershey Medical Center Hershey Pennsylvania 17033

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00815880, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 23, 2023 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00815880 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →