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Clinical Trials in China / NCT07003399
Recruiting Observational

Diaphragmatic Function and Respiratory Drive in OSA and COPD

NCT07003399 · tracked via the Priya Life Science China tracker
Sponsor
Nanjing Medical University
Phase
Observational
Started
2025-01-01
Last updated
2025-06-25

Condition(s) studied

Obstructive Sleep Apnea

Investigational drug(s) / intervention(s)

Diaphragmatic Ultrasound and EMG Assessment

Diaphragmatic Ultrasound and EMG Assessment: Non-invasive assessment of diaphragmatic morphofunction and respiratory drive using ultrasound imaging and diaphragm electromyography (EMG). This evaluation will be performed once per participant without any therapeutic intervention.

Study summary

This cross-sectional observational study aims to assess the diaphragmatic morphofunction and respiratory drive characteristics among patients with obstructive sleep apnea (OSA), chronic obstructive pulmonary disease (COPD), overlap syndrome (OS), and healthy controls. Using ultrasound imaging and surface diaphragm electromyography (EMGdi), the study will explore group differences in diaphragmatic morphology, function, and respiratory drive indicators, and evaluate their clinical significance in disease differentiation and severity assessment.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. Patients aged between 18 and 80 years. 2. For OSA Group: Diagnosed obstructive sleep apnea with AHI ≥ 5 events/hour based on overnight polysomnography. 3. For COPD Group: Diagnosed chronic obstructive pulmonary disease based on GOLD guidelines. 4. For Overlap Group: Diagnosed both OSA (AHI ≥ 5) and COPD. 5. For Control Group: Healthy volunteers with no known respiratory diseases or sleep disorders. 6. Ability and willingness to provide informed consent for participation in the study. Exclusion Criteria: 1. Severe cardiovascular diseases (e.g., unstable angina, heart failure NYHA III/IV). 2. Severe hepatic or renal insufficiency. 3. Neuromuscular diseases affecting respiratory muscles. 4. Recent upper airway or thoracic surgery (within 3 months). 5. Pregnancy or breastfeeding. 6. Participants who cannot complete assessments due to cognitive impairment or poor cooperation.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The First Affiliated Hospital of Nanjing Medical University Nanjing Jiangsu Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07003399 on ClinicalTrials.gov ↗ ← All trials in China