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Completed Phase 3 Interventional Results available

Furoscix Real-World Evaluation for Decreasing Hospital Admissions in Heart Failure

ClinicalTrials.gov ID: NCT03458325

Public ClinicalTrials.gov record NCT03458325. 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 Oct 19, 2026, 2:31 PM EDT

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

Official title

Economic Impact of Reducing Hospital Admissions for Patients Presenting to the Emergency Department With Worsening Heart Failure: An Adaptive Clinical Trial of Furoscix Infusor

Brief summary

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

The study is to evaluate the safe admission avoidance and the overall economic impact associated with management of worsening HF using the drug-device combination product, the Furoscix Infusor, outside the hospital setting in patients initially presenting to the emergency department. The study drug, Furoscix (furosemide injection 8 mg/ml), is a furosemide solution buffered to a neutral pH containing 80 mg/10 mL for subcutaneous administration over 5 hours via the Furoscix Infusor. The study objectives are: 1. To evaluate differences in healthcare resource utilization and direct medical costs for patients treated with the Furoscix Infusor outside the hospital versus patients receiving intravenous furosemide for ≤ 72 hours in the hospital setting for 30 days post-discharge from the emergency department. 2. To evaluate the safety of Furoscix administered outside the hospital. 3. To evaluate and describe quality of life and patient satisfaction for patients who receive the Furoscix Infusor outside the hospital setting.

Study identification

NCT ID
NCT03458325
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
scPharmaceuticals, Inc.
Industry
Enrollment
27 participants

Conditions and interventions

Conditions

Interventions

Combination Product

Eligibility (public fields only)

Age range
18 Years to 80 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
Nov 12, 2020 (Actual)
Primary completion
Jun 24, 2021 (Actual)
Completion
Jun 24, 2021 (Actual)
Last update posted
Feb 24, 2023

2020 – 2021

United States locations

U.S. sites
8
U.S. states
8
U.S. cities
8
Facility City State ZIP Site status
Olive View - UCLA Medical Center Sylmar California 91342 —
Bridgeport Hospital Bridgeport Connecticut 06610 —
Tampa General Hospital Tampa Florida 33606 —
Ascension St. Vincent Heart Center Indianapolis Indiana 46260 —
Unity Point Health Des Moines Iowa 50309 —
University of Minnesota Medical Center Minneapolis Minnesota 55422 —
Moses H. Cone Memorial Hospital Greensboro North Carolina 27401 —
Abington Hospital - Jefferson Health Abington Pennsylvania 19001 —

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 NCT03458325, 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 Feb 24, 2023 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03458325 live on ClinicalTrials.gov.

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