Respiratory Muscle Fatigue and Lower Extremity Muscle Oxygenation
Recruiting now · Not applicable
Conditions studied: COPD
In brief
In our study, changes in vastus lateralis muscle oxygenation will be evaluated with the Moxy device, a functional infrared oxygen measurement device, during the inspiratory muscle fatigue protocol in COPD cases and the healthy control group.
Key facts
- Study ID
- NCT06217276
- Run by
- Istanbul Medipol University Hospital
- People needed
- 30
- Starts
- 2024-01-20
- Expected to finish
- 2026-01-15
- Last updated by the study team
- 2025-05-01
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Having a diagnosis of Stage 2-3 COPD according to the following clinical diagnostic criteria according to the American Thoracic and European Respiratory Societies (ATS-ERS).
- Having been using the same medications for the last 4 weeks
You may not qualify if…
- Patients with severe comorbid diseases, unstable coronary artery disease, collagen vascular diseases and requiring high-flow oxygen therapy (˃ 3-4 L\\min).
- Presence of any vascular problem that may affect lower extremity muscle oxygenation
- Presence of another respiratory system disease other than COPD
- Patients who have had an acute COPD exacerbation in the last 4 weeks
- Patients experiencing COPD exacerbations during the study protocol
- Presence of fatty tissue or scar tissue at the measurement points, which may impair the measurement quality.
- Have already participated in another clinical trial within the last 30 days that may affect the results of the study.
- Inclusion Criteria for Healthy Cases
- Being over 18 years of age
- Not having any diagnosed chronic disease
- Not being a smoker
Where it is running
- Yedikule Chest Disease Hospital — Istanbul, Zeytinburnu, Turkey (Türkiye) (enrolling)
Full record on ClinicalTrials.gov
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