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NCT05124015

Exercise Capacity Respiratory Muscle Strength Dyspnea and Physical Activity in Pediatric Pulmonary Arterial Hypertension

Completed Last updated 25 March 2025
What this trial tests

trial in Pulmonary Arterial Hypertension in 33 participants. Completed in 1 January 2022.

Timeline
10 November 2019
Primary endpoint
10 April 2021
1 January 2022

Quick facts

Lead sponsorGazi University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment33
Start date10 November 2019
Primary completion10 April 2021
Estimated completion1 January 2022
Sites1 location across Turkey (Türkiye)

Conditions studied

Sponsor

Gazi University

Who can join

Adults 6 to 18, any sex, with Pulmonary Arterial Hypertension. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary aim of this study was to evaluate exercise capacity, respiratory muscle strength, pulmonary function, dyspnea and physical activity levels in pediatric PAH patients and compare them with healthy controls. The secondary aim of the study was; To investigate the relationship of dyspnea with exercise capacity, respiratory muscle strength, respiratory functions, physical activity and blood count parameters in pediatric PAH patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Pulmonary Arterial Hypertension

Currently open trials in the same condition.

Other Gazi University trials

Trials by the same sponsor.

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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/NCT05124015.

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