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NCT07430189: PuRe-axSpA

Multimodal Pulmonary Rehabilitation in Radiographic Axial Spondyloarthritis

Completed NA Last updated 25 February 2026
What this trial tests

NA trial testing Multimodal Pulmonary Rehabilitation in Axial Spondyloarthritis (AxSpA) in 20 participants. Completed in 30 September 2020.

Timeline
30 May 2018
Primary endpoint
30 September 2020
30 September 2020

Quick facts

Lead sponsorBalikesir University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment20
Start date30 May 2018
Primary completion30 September 2020
Estimated completion30 September 2020
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Balikesir University

Who can join

Adults 18 to 75, any sex, with Axial Spondyloarthritis (AxSpA). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This prospective pilot study aims to evaluate the efficacy of a structured 8-week multimodal pulmonary rehabilitation (PR) program specifically designed for patients with radiographic axial spondyloarthritis (r-axSpA). The study assesses the impact of a composite intervention incorporating aerobic conditioning, resistance training, flexibility protocols, and targeted diaphragmatic breathing on functional exercise capacity, dyspnea severity, and pulmonary function.

Publications & conference data

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

Verify or expand the search:

Other recruiting trials for Axial Spondyloarthritis (AxSpA)

Currently open trials in the same condition.

Other Balikesir University 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/NCT07430189.

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