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Sivelestat sodium regulates cellular inflammatory factors and immune markers in the treatment of acute severe pancreatitis

Sivelestat sodium regulates cellular inflammatory factors and immune markers in the treatment of acute severe pancreatitis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097354
Enrollment
Unknown
Registered
2025-02-18
Start date
2024-05-05
Completion date
Unknown
Last updated
2025-02-24

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

Conditions

Severe pancreatitis

Interventions

Control Group:Fasting, anti-infection, replenishing blood volume, inhibiting gastric acid secretion, gastrointestinal decompression, maintaining water and electrolyte balance
Group A:Fasting, anti-infection, blood volume supplementation, inhibition of gastric acid secretion, gastrointestinal decompression, maintenance of water and electrolyte balance +0.1mg/kg*h injection
Group B:Fasting, anti-infection, blood volume supplementation, inhibition of gastric acid secretion, gastrointestinal decompression, maintenance of water and electrolyte balance +0.2mg/kg*h Injection

Sponsors

Dazhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Meets the diagnostic criteria for acute pancreatitis in the Chinese Guidelines for the Diagnosis and Treatment of Acute Pancreatitis (2021) (with the following 2 or more points): a. persistent upper abdominal pain, b. serum amylase and/or lipase concentration at least 3 times higher than the upper limit of normal, c. abdominal imaging examination results show imaging changes consistent with acute pancreatitis; Admitted within 24 hours of onset; Age range from 20 to 65 years old; All patients have given informed consent and voluntarily joined this study, and have been approved by the hospital ethics committee; Complies with the indications for Sivelestat Sodium.

Exclusion criteria

Exclusion criteria: Other intestinal diseases, pregnancy or lactation, malignant tumor, Coagulopathy and hemorrhagic disease, intestinal surgery and intestinal adhesion Poor compliance or incomplete clinical data, accompanied by communication disorders and mental illness.

Design outcomes

Primary

MeasureTime frame
TNF-a;IL-6;IL-10;

Secondary

MeasureTime frame
CRP;IL-1ß;CD4+;CD8+;CD4+/CD8+;

Countries

China

Contacts

Public ContactWenlai Zhou

Dazhou Central Hospital

702075218@qq.com+86 189 8019 9189

Outcome results

None listed

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