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Risk Identification Factors for Pulmonary Function Impairment in AIDS Patients Recovered From Severe Pneumonia

Pneumonia Clinical Trial

Official title:
Study on Risk Identification Factors for Lung Function Impairment in AIDS Patients Recovered From Severe Pneumonia

Clinical Trial 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.

Clinical Trial Description

This is a prospective, single-center, non-randomized, clinical observational cohort study. It involves monitoring lung function at discharge (baseline, 0w), and at the 4th, 8th, 12th, 24th, and 48th weeks in patients recovering from severe pneumonia with AIDS. Basic demographic data, HIV RNA quantification, routine blood tests, blood biochemistry, arterial blood gas results, oxygenation index, immune function (CD3+, CD4+, CD8+ T cell counts), and imaging studies are also collected. Multifactorial logistic regression analysis is used to screen for clinical predictors of lung function decline in patients recovering from severe pneumonia ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06137196
Study type Observational
Source Guangzhou 8th People's Hospital
Contact Linghua Li, PhD
Phone +862083710825
Email llheliza@126.com
Status Recruiting
Phase
Start date November 1, 2023
Completion date November 1, 2027
View Details
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