Clinical Trials in China / NCT06137196
Recruiting
Observational
Risk Identification Factors for Pulmonary Function Impairment in AIDS Patients Recovered From Severe Pneumonia
NCT06137196 · tracked via the Priya Life Science China tracker
Condition(s) studied
AIDSPneumonia
Study summary
Screening for risk factors related to lung function impairment in patients who have recovered from AIDS with severe pneumonia, to provide clinical evidence for early identification and intervention of lung function damage in this population.
Eligibility
Inclusion Criteria:
1. Confirmed HIV infection;
2. Progression to the AIDS stage: CD4+ count \<200 cells/µL and/or occurrence of opportunistic infections associated with AIDS;
3. Age between 18 to 65 years;
4. Meet the diagnostic criteria for severe pneumonia, with reference to the 2021 treatment guidelines for community-acquired pneumonia developed by the American Thoracic Society (ATS) and the Infectious Diseases Society of America (IDSA).
Exclusion Criteria:
1. Concurrent central nervous system lesions, severe liver disease, or cirrhosis;
2. Concurrent AIDS-related or non-related tumors;
3. Women who are pregnant or breastfeeding;
4. Presence of serious underlying diseases such as heart, lung, liver, kidney, etc.;
5. Alcohol abuse or drug use;
6. The researcher believes that the overall condition of the subject affects the evaluation and completion of the trial
Primary outcome measure(s)
- Obstructive Ventilatory Dysfunction — 12 weeks
FEV1(Forced Expiratory Volume in One Second )to FVC (Forced Vital Capacity ) Ratio
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Guangzhou Eighth People's Hospital, Guangzhou Medical University | Guangzhou | Guangdong | Recruiting |
More Guangzhou 8th People's Hospital trials in China
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 NCT06137196 on ClinicalTrials.gov ↗ ← All trials in China