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NCT00124137 · ClinicalTrials.gov registry record · NA
Ultrafiltration Versus Intravenous (IV) Diuretics for Patients Hospitalized for Acute Decompensated Heart Failure: (UNLOAD)
A NA study, sponsored by Nuwellis.
- Completed
- Registry status
- NA
- Development phase
- 200
- Enrollment target
NCT00124137: Completed NA study, sponsored by Nuwellis.
NCT00124137 is a NA study that has completed, run by Nuwellis. The registered enrollment target is 200 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00124137, a NA study, has completed, sponsored by Nuwellis.
- COMPLETED
- Registry status
- NA
- Development phase
- 200 participants
- Enrollment target
Study Summary
The purpose of this study is to compare patients who are suffering from heart failure and who are fluid overloaded to determine if ultrafiltration (UF) can remove more of the extra fluid as measured by weight loss while in the hospital and improve the patient's breathing.
Interventions
- DEVICE Aquadex system
- DRUG IV diuretic
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2004-04 |
| Est. Completion | 2005-10 |
| Phase | NA |
What the finished NCT00124137 record still lists
NCT00124137 is an interventional study that assigns participants to a tested intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (86% lower).
The record links to 0 conditions, and to 2 interventions - of which Aquadex system is the first listed.
NCT00124137 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00124137 about?
NCT00124137 is a clinical study titled "Ultrafiltration Versus Intravenous (IV) Diuretics for Patients Hospitalized for Acute Decompensated Heart Failure: (UNLOAD)". The purpose of this study is to compare patients who are suffering from heart failure and who are fluid overloaded to determine if ultrafiltration (UF) can remove more of the extra fluid as measured by weight loss while in the hospital and improve the patient's breathing.
What is the current status of trial NCT00124137?
This trial is currently completed. It is a NA study. The enrollment target is 200 participants. The study started on 2004-04. Estimated completion is 2005-10.
What interventions are being tested in trial NCT00124137?
The interventions under investigation include: Aquadex system (DEVICE), IV diuretic (DRUG).
Who is sponsoring clinical trial NCT00124137?
This trial is sponsored by Nuwellis, which has 7 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00124137's enrollment target sits among peer trials
200 506th of 2000 higher than 1,434 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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