RecruitingPhase 3NCT07208591
To Evaluate The Safety and Efficacy of STSA-1002 Injection in Patients With Acute Respiratory Distress Syndrome
Studying Acute lung injury
Last synced from ClinicalTrials.gov
ℹ
Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Staidson (Beijing) Biopharmaceuticals Co., Ltd
- Principal Investigator
- Bin M.D. CaoChina-Japan Friendship Hospital
- Intervention
- STSA-1002 injection(drug)
- Enrollment
- 406 target
- Eligibility
- 18-85 years · All sexes
- Timeline
- 2025 – 2026
Study locations (15)
- China-Japan Friendship Hospital, Beijing, Beijing Municipality, China
- The First Affiliated Hospital of Xiamen University, Xiamen, Fujian, China
- The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China
- The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China
- The Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China
- The First Affiliated Hospital of Henan University of Science and Technology, Luoyang, Henan, China
- Henan Provincial People's Hospital, Zhengzhou, Henan, China
- The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China
- Wuhan Central Hospital, Wuhan, Hubei, China
- Xiangtan Central Hospital, Xiangtan, Hunan, China
- The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China
- Weifang People's Hospital, Weifang, Shandong, China
- Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, Chengdu, Sichuan, China
- Dazhou Central Hospital, Dazhou, Sichuan, China
- Hangzhou First People's Hospital, Hangzhou, Zhejiang, China
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT07208591 on ClinicalTrials.govOther trials for Acute lung injury
Additional recruiting or active studies for the same condition.
- RECRUITINGNANCT06526598Inspiratory Effort-Targeted Pressure Support Ventilation (IT-PSV) TrialCapital Medical University
- RECRUITINGNANCT07380789Comprehensive Multicenter Study on the Management of Acute Pain Following Thoracic Combat-Related Trauma in UkraineLviv National Medical University
- RECRUITINGPHASE2, PHASE3NCT07342205A Study on the Treatment of Patients With Acute Lung Injury Caused by Sepsis Through Microbiota TransplantationShanghai University of Traditional Chinese Medicine
- RECRUITINGPHASE2NCT06513949Anti-CD14 Treatment With IC14 in Hospitalized ARDS PatientsImplicit Bioscience
- RECRUITINGPHASE2NCT06703073JUST BREATHE, Breathing Life Into Innovative Therapies for ARDS (Master Record)PPD Development, LP
- RECRUITINGPHASE1, PHASE2NCT07413978A Clinical Trial of Human Umbilical Cord Mesenchymal Stem Cell Injection for the Treatment of Severe Acute Respiratory Distress SyndromeChangchun Tuohua Pharmaceutical Co., Ltd.
- RECRUITINGNANCT06772025A Study to Understand How Cardiac Surgery-associated Acute Kidney Injury Develops in Participants Who Undergo Heart Surgery With the Use of Heart-lung MachineBayer
- RECRUITINGNCT07100860The Effect of Single Lung Ventilation Duration on Postoperative Pulmonary Complications in Thoracic SurgeryDr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital