Phase 2Not yet recruitingGeroscience intervention

Urolithin A Supplementation During Pulmonary Rehabilitation in Patients With COPD (SUPRA-COPD)

The Supplementation With Urolithin A During Pulmonary Rehabilitation in COPD (SUPRA-COPD) Trial

Sponsor
Bryan A. Ross (Academic or other)
Enrolment
198 planned
Conditions
Chronic Obstructive Pulmonary Disease (COPD)
Interventions
Urolithin A; Placebo
Ages
adults, older adults
Registry
NCT07871357

Full record on ClinicalTrials.gov

From the registry

SUPRA-COPD is a multicenter triple-blind, parallel arm, placebo-controlled randomized controlled trial investigating the efficacy and safety of Urolithin A supplementation during pulmonary rehabilitation in patients with COPD. The goal of the SUPRA-COPD study is to investigate whether Urolithin A supplementation during pulmonary rehabilitation in patients with COPD improves exercise tolerance, along with several other clinically important outcomes, above and beyond pulmonary rehabilitation participation alone. Study participation will be approximately 14 weeks and involves in-person visits evaluating exercise tolerance before and after PR.

Primary outcomes

  • Change in exercise endurance time (constant work rate exercise test, CWRET)

History

  1. Primary completion expected

  2. Expected to start

  3. Registered