ALI/ARDS Clinical Sub-phenotyping Study

RecruitingOBSERVATIONAL
Enrollment

1,500

Participants

Timeline

Start Date

December 14, 2023

Primary Completion Date

December 31, 2025

Study Completion Date

December 31, 2025

Conditions
Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS)
Interventions
PROCEDURE

Collect peripheral blood and bronchoalveolar lavage fluid

"Peripheral venous blood will be collected and stored from the study participants at a total of five time points: Day 0, Day 1, Day 2, Day 3 after admission to the ICU, and the day of ICU discharge/death. The collection will be conducted after assessing the patients' eligibility for ARDS diagnosis. Each time point will involve the collection of one tube of peripheral venous blood, totaling 5 mL per sample.~Within 24 hours after patients' admission to the ICU and meeting the assessment criteria for ARDS diagnosis, bronchoalveolar lavage fluid (BALF) will be collected and retained, totaling 10 mL."

Trial Locations (1)

Unknown

RECRUITING

Jingen Xia, Beijing

All Listed Sponsors
lead

China-Japan Friendship Hospital

OTHER