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Clinical Trial

Use of a Novel SUBCUTaneous Preparation of Furosemide to Facilitate Early Supported Discharge of Patients With Heart Failure

NCT: NCT05419115 · COMPLETED

NCT IDNCT05419115
StatusCOMPLETED
Start Date2022-11-17
Completion2026-03-01

Brief Summary

To investigate whether an early supported discharge strategy for patients admitted to hospital because of HF, using a pH neutral subcutaneous (SC) furosemide formulation (SQINFurosemide) at home (delivered by non-CE marked SQINInfusor), compared to a usual care strategy with intravenous (IV) furosemide in hospital, results in an increased number of days spent alive and out of hospital (DAOH) at 30 days.

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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