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NCT01457053 · ClinicalTrials.gov registry record · NA
Assessment of Coronary Flow Reserve in Heart Failure Patients After Ultrafiltration Versus Diuretics
A NA study, sponsored by University of Cincinnati.
- Terminated
- Registry status
- NA
- Development phase
- 4
- Enrollment target
NCT01457053: Clinical Trial NA study, sponsored by University of Cincinnati.
NCT01457053 is a NA study that was terminated before completion, run by University of Cincinnati. The registered enrollment target is 4 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01457053, a NA study, was terminated before completion, sponsored by University of Cincinnati.
- TERMINATED
- Registry status
- NA
- Development phase
- 4 participants
- Enrollment target
Study Summary
The purpose of this research study is to compare the effects (good and bad) of ultrafiltration treatment with standard intravenous (in your vein) diuretic therapy (furosemide, torsemide, bumetanide) on your heart function and blood flow.
Primary Outcome
Evaluate the effects of ultrafiltration (UF) compared to intravenous diuretic therapy on myocardial blood flow (MBF) and coronary flow reserve (CFR), as assessed by positron emission tomography (PET), in patients with acutely decompensated heart failure (ADHF).
Interventions
- OTHER Ultrafiltration
- DRUG Loop diuretics (furosemide, torsemide, bumetanide)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 4 participants |
| Start Date | 2011-11 |
| Est. Completion | 2013-05 |
| Phase | NA |
Why NCT01457053 stopped before completion
NCT01457053 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 4 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).
The record links to 0 conditions, and to 2 interventions - of which Ultrafiltration is the first listed.
NCT01457053 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01457053 about?
NCT01457053 is a clinical study titled "Assessment of Coronary Flow Reserve in Heart Failure Patients After Ultrafiltration Versus Diuretics". The purpose of this research study is to compare the effects (good and bad) of ultrafiltration treatment with standard intravenous (in your vein) diuretic therapy (furosemide, torsemide, bumetanide) on your heart function and blood flow.
What is the current status of trial NCT01457053?
This trial is currently terminated. It is a NA study. The enrollment target is 4 participants. The study started on 2011-11. Estimated completion is 2013-05.
What interventions are being tested in trial NCT01457053?
The interventions under investigation include: Ultrafiltration (OTHER), Loop diuretics (furosemide, torsemide, bumetanide) (DRUG).
Who is sponsoring clinical trial NCT01457053?
This trial is sponsored by University of Cincinnati, which has 245 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01457053's enrollment target sits among peer trials
4 1996th of 2000 higher than 5 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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