Intermittent Hypoxemia, Lung Function Decline, Morbidity, and Mortality in COPD (PROSA Study).
- Disease/Condition
- Chronic Obstructive Pulmonary Disease (COPD)
- Drug/Device/Intervention
- No active intervention, but observational follow-up
- Study type
- Observational
- Intervention type
- other
- Primary sponsor
- Universitätsklinikum Hamburg-Eppendorf
- Location
- Hamburg, Germany
- Phase
- N/A
- Start date
- Mar 01, 2024
- End date
- Sep 30, 2029
- Enrollment
- 148 participants
Difference in FEV1(% of LLN) between baseline and end-of-follow-up
This study aims to analyze if patients with chronic obstructive lung disease who experience a
 decline of blood oxygen saturation during physical exercise have a disease course different
 from that of COPD patients who do not experience a decline in blood oxygen saturation during
 exercise. Patients will be followed for a total of 3 years.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06265623
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06265623 through Pure Global AI's free database. This phase not specified trial is sponsored by Universitätsklinikum Hamburg-Eppendorf and is currently Not yet recruiting. The study focuses on Chronic Obstructive Pulmonary Disease (COPD). Target enrollment is 148 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.