drugset / Trial / NCT05769738

The Addition of Inhaled Furosemide to Standard Treatment of COPD Exacerbation

NCT05769738

Phase 3 Unknown 200 enrolled American University of Beirut Medical Center
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The goal of this randomized controlled trial is to determine the effect of adding inhaled furosemide to the known treatment of patient with Chronic obstructive pulmonary disease (COPD) exacerbation. It primarily aims at studying its effect on: 1. Relief of dyspnea sensation 2. Length of hospital stay Participants will be receiving the standard therapy of COPD exacerbation plus either inhaled furosemide or inhaled saline over 3 days. They will be asked to: * Perform spirometry * Fill in dyspnea score * Do arterial blood gases (ABGs)

Timeline

Start
2023-03
Primary completion
2024-12
Completion
2024-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Furosemide Other / unclassified 40 mg Inhaled