Prevention of Ulinastatin on Acute Respiratory Distress Syndrome (ARDS)
Launched by PEKING UNIVERSITY THIRD HOSPITAL · Mar 19, 2017
Trial Information
Current as of May 27, 2025
Completed
Keywords
ClinConnect Summary
Since strategies were applied in intensive care medicine, including low tidal volume ventilation, fluid resuscitation, use of antibiotics, restrictive transfusion strategy and bundle of ventilator therapy, the incidence of Acute Respiratory Distress Syndrome (ARDS) has been decreased recent years. However, the mortality of severe ARDS is still higher to 45%. Few medications did were indicated to be effective in working on development of ARDS. Different with other disease, ARDS were difficult to prevent in its later stage like a domino effect. The medication interventions are all used after ...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patients should be more than 18 years old
- • Patients are expected to living within 72 hours of ICU admission
- • Patients' Lung Injury Prediction Score (LIPS) more than 4 and got at least 1 risk factors as below: bacteremia, sepsis or sepsis shock, pneumonia, multiple fractures, pulmonary contusion, aspiration, multiple blood transfusion, severe acute pancreatitis.
- • Exclusion Criteria: Patients will be excluded when they are
- • diagnosed as ARDS
- • without written informed consent
- • with HIV infection
- • with other immunologic deficiency (leukaemia, immune deficiency syndrome, etc)
- • with organ transplantation or bone marrow transplantation
- • with chronic pulmonary disease (except for Chronic Obstructive Pulmonary Disease (COPD) or asthma)
- • with angitis
- • with neutropenia (except for secondary to sepsis)
- • using granulocyte-macrophage colony-stimulating factor or granulocyte colony-stimulating factor
- • using asprin or clopidogrel
- • using glucocorticoid
- • withdrawing treatment
- • treated by Xuebijing, thymosin, or intravenous immunoglobulin 1 month before enrollment
- • enrolled in other clinical trials 3 months before enrollment
- • being pregnancy
- • being lactation
About Peking University Third Hospital
Peking University Third Hospital is a leading medical institution in China, renowned for its commitment to advanced healthcare, innovative research, and comprehensive clinical services. As a prominent sponsor of clinical trials, the hospital emphasizes the integration of cutting-edge scientific research with patient-centered care to enhance therapeutic outcomes. With a multidisciplinary approach, the institution fosters collaboration among top-tier medical professionals and researchers, striving to contribute to the global medical community through rigorous clinical studies that address pressing health challenges. Its dedication to ethical standards and regulatory compliance ensures the safety and efficacy of new treatments, ultimately aiming to improve patient care and outcomes on both a national and international scale.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Beijing, , China
Nanning, Guangxi, China
Nanning, Guangxi, China
Beijing, Beijing, China
Beijing, Beijing, China
Zhengzhou, Henan, China
Dalian, Liaoning, China
Shenzhen, Guangdong, China
Beijing, Beijing, China
Beijing, Beijing, China
Cangzhou, Hebei, China
Zibo, Shandong, China
Patients applied
Trial Officials
Xi Zhu, M.D.
Principal Investigator
Peking University Third Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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