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NCT00815880 · ClinicalTrials.gov registry record · NA
C-Pulse IDE Feasibility Study- A Heart Assist System
A NA study, sponsored by Nuwellis.
- Completed
- Registry status
- NA
- Development phase
- 21
- Enrollment target
NCT00815880 is a NA study that has completed, run by Nuwellis. The registered enrollment target is 21 participants.
The verdict
NCT00815880, a NA study, has completed, sponsored by Nuwellis.
- COMPLETED
- Registry status
- NA
- Development phase
- 21 participants
- Enrollment target
Study Summary
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.
Interventions
- DEVICE C-Pulse™ (Implantable Counterpulsation Therapy)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 21 participants |
| Start Date | 2008-09-10 |
| Est. Completion | 2018-09-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00815880
The ClinicalTrials.gov registry entry for NCT00815880 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 21 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Nuwellis, which has 7 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which C-Pulse™ (Implantable Counterpulsation Therapy) is the first listed.
NCT00815880 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00815880 about?
NCT00815880 is a clinical study titled "C-Pulse IDE Feasibility Study- A Heart Assist System". 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 fun...
What is the current status of trial NCT00815880?
This trial is currently completed. It is a NA study. The enrollment target is 21 participants. The study started on 2008-09-10. Estimated completion is 2018-09-07.
What interventions are being tested in trial NCT00815880?
The interventions under investigation include: C-Pulse™ (Implantable Counterpulsation Therapy) (DEVICE).
Who is sponsoring clinical trial NCT00815880?
This trial is sponsored by Nuwellis, which has 7 total clinical trials registered on ClinicalTrials.gov.
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