Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02579057 · ClinicalTrials.gov registry record · Phase 2
Sub-Q Versus IV Furosemide in Acute Heart Failure
A Phase 2 study, sponsored by Johns Hopkins University.
- Completed
- Registry status
- Phase 2
- Development phase
- 40
- Enrollment target
NCT02579057: Completed Phase 2 study, sponsored by Johns Hopkins University.
NCT02579057 is a Phase 2 study that has completed, run by Johns Hopkins University. The registered enrollment target is 40 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02579057, a Phase 2 study, has completed, sponsored by Johns Hopkins University.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 40 participants
- Enrollment target
Study Summary
This study evaluates the clinical efficacy of subcutaneously administered Furosemide Injection Solution versus intravenous administration of Furosemide Injection, United States Pharmacopeia (USP) in adult patients presenting to a heart failure clinic with decompensated heart failure. Half of the patients will receive a subcutaneously administered Furosemide Injection Solution; the other half will receive an intravenous administration of Furosemide Injection.
Primary Outcome
The volume of urine produced in milliliters over the 6 hours after drug delivery will be measured.
Interventions
- DRUG Furosemide Injection Solution (SCP-101)
- DRUG Furosemide Injection Solution, USP
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2016-02 |
| Est. Completion | 2017-07 |
| Phase | Phase 2 |
What the finished NCT02579057 record still lists
NCT02579057 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower).
The record links to 0 conditions, and to 2 interventions - of which Furosemide Injection Solution (SCP-101) is the first listed.
NCT02579057 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02579057 about?
NCT02579057 is a clinical study titled "Sub-Q Versus IV Furosemide in Acute Heart Failure". This study evaluates the clinical efficacy of subcutaneously administered Furosemide Injection Solution versus intravenous administration of Furosemide Injection, United States Pharmacopeia (USP) in adult patients presenting to a heart failure clinic with decompensated heart failure. Half of the pat...
What is the current status of trial NCT02579057?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 2016-02. Estimated completion is 2017-07.
What interventions are being tested in trial NCT02579057?
The interventions under investigation include: Furosemide Injection Solution (SCP-101) (DRUG), Furosemide Injection Solution, USP (DRUG).
Who is sponsoring clinical trial NCT02579057?
This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02579057's enrollment target sits among peer trials
40 1362nd of 2000 higher than 542 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT01306019 · 40 participants · Phase 1
Lentiviral Gene Transfer for Treatment of Children Older Than Two Years of Age With X-Linked Severe Combined Immunodeficiency (XSCID)
- NCT01608152 · 40 participants
Development of a Video Game for the Improvement of Outcomes in Stem Cell Transplant Survivors
- NCT01668082 · 40 participants · NA
An Investigation of Brain Tumor Metabolism in Patients Undergoing Surgical Resection
- NCT02015013 · 40 participants · Phase 2
Hematopoietic Stem Cell Mobilization in Idiopathic CD4 Lymphocytopenia Patients and Healthy Controls for the Study of T Cell Maturation and Trafficking in Murine Models
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia