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NCT03177837

Effect of Acetazolamide on Exercise Performance in Patients With Respiratory Disease at Altitude

Completed Phase 4 Last updated 16 August 2019
What this trial tests

Phase 4 trial testing ACETAZOLAMIDE oral capsule in Chronic Obstructive Pulmonary Disease in 176 participants. Completed in 2 August 2018.

Timeline
24 May 2017
Primary endpoint
2 August 2018
2 August 2018

Quick facts

Lead sponsorUniversity of Zurich
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposeprevention
Enrollment176
Start date24 May 2017
Primary completion2 August 2018
Estimated completion2 August 2018
Sites1 location across Kyrgyzstan

Drugs / interventions tested

Conditions studied

Sponsor

University of Zurich

Who can join

Adults 18 to 75, any sex, with Chronic Obstructive Pulmonary Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

In this trial, the investigators will evaluate the effect of acetazolamide (375 mg per day) vs. placebo on exercise performance at altitude in patients with COPD.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Effects of acetazolamide on exercise performance in patients with COPD going to high altitude: randomised controlled trial.
    Kind RF, Furian M, Buergin A, Scheiwiller PM, et al · · 2025 · cited 3× · PMID 39834599 · DOI 10.1183/23120541.00767-2024

Verify or expand the search:

Other trials of ACETAZOLAMIDE oral capsule

Trials testing the same drug.

Other recruiting trials for Chronic Obstructive Pulmonary Disease

Currently open trials in the same condition.

Other University of Zurich trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03177837.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing