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Search / Trial NCT03089957

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

Acute Respiratory Distress Syndrome Critical Illness Randomized Controlled Trial Ulinastatin

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.

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

0 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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