Overview
Treatment of ARDS With Sivelestat Sodium
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2024-07-30
2024-07-30
Target enrollment:
0
0
Participant gender:
All
All
Summary
Neutrophil elastase (NE) released by neutrophils play an important role in inflammatory cascade and lung tissue injury of ARDS.Inhibition of NE is expected to prevent the pathophysiological process of ARDS and alleviate lung injury. Siverestat sodium is a specific inhibitor of NE, which has been proved by basic and observational clinical studies to be effective in alleviating lung injury of ARDS, but there is a lack of prospective multi-center randomized controlled clinical trials.Therefore, this study was intended to evaluate the efficacy of sivelestat sodium in the treatment of ARDS patients with SIRS in a multicenter randomized controlled clinical trialPhase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Sichuan Provincial People's HospitalTreatments:
Sivelestat
Criteria
Inclusion Criteria:1. Males and females > 18 years old and <75 years old (non-pregnant, non-lactating
females).
2. Patients fulfilled the Berlin diagnostic criteria of acute respiratory distress
syndrome, with a arterial oxygen partial pressure (PaO2) to fraction of inspired
oxygen (FiO2) between 150 mmHg and 300 mmHg.
3. Signed written informed consent has been obtained
Exclusion Criteria:
1. History of chronic respiratory disease
2. Single cardiogenic pulmonary edema
3. Apach2 score ≥21 points
4. Complicated with end-stage disease, or poor prognosis judged by the clinical doctor in
charge
5. ARDS course>3 days
6. Agranulocytosis or receiving immunosuppressive agents or high doses of corticosteroids
(methylprednisolone>40mg/day)
7. Pregnancy or breastfeeding
8. Participated in this study
9. Do not agree to participate in this experiment