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Effect of sivilastat sodium on immune function in patients with acute lung injury with sepsis

Effect of sivilastat sodium on immune function in patients with acute lung injury with sepsis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400092435
Enrollment
Unknown
Registered
2024-11-15
Start date
2024-07-19
Completion date
Unknown
Last updated
2024-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

sepsis acute lung injury

Interventions

Sivilastat sodium group:None
Without Sivilastat sodium group:

Sponsors

the 908th Hospital of Chinese Logistical Support Force
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Meet sepsis 3.0 criteria (infection or suspected infection + sequential organ failure score (SOFA) = 2); Oxygenation index= 300mmHg; Voluntary participation in this trial and informed consent.

Exclusion criteria

Exclusion criteria: Women who are pregnant, nursing, or may be pregnant; Patients who are allergic to the study drug; less than 7 days of medication and less than 7 days of hospital stay; Patients with a history of the following diseases: patients with severe heart, lung, renal, and hepatic insufficiency or immune disorders; Patients who have been treated with hormones, immunosuppressants and other drugs or have had organ transplantation within the past 6 months.

Design outcomes

Primary

MeasureTime frame
PaO2/FiO2;Duration of mechanical ventilation;ICU duration and hospital stay ;

Secondary

MeasureTime frame
Free DNA;Neutrophil elastase;prothrombin time;activated partial thromboplastin time;thrombin time;fibrinogen;fibrin degradation products;D-Dimer;antithrombin ;neutrophil-to-lymphocyte ratio;INF-?;Transforming growth factor beta;

Countries

China

Contacts

Public ContactSong Jingchun

Department of Critical Care Medicine, the 908th Hospital of Chinese Logistical Support Force

songjingchun@126.com+86 189 7089 9900

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026