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A randomized controlled study on the effect of compound leucine granules on the nutritional status and prognosis of patients with pancreatitis

A randomized controlled study on the effect of compound leucine granules on the nutritional status and prognosis of patients with pancreatitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110455
Enrollment
Unknown
Registered
2025-10-14
Start date
2025-10-15
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

Pancreatitis

Interventions

intervention group of acute pancreatitis:Conventional therapy plus Compound Leucine Granules (oral, three times daily for 7 days)
Control group of acute pancreatitis:Conventional therapy plus placebo (oral, three times daily for 7 days)
Intervention group of Chronic pancreatitis:Conventional therapy plus Compound Leucine Granules (oral, three times daily for 7 days)
Control group of chronic pancreatitis:Conventional therapy plus placebo (oral, three times daily for 7 days)

Sponsors

The First Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.For patients with mild to moderate acute pancreatitis or chronic pancreatitis in the Hepatobiliary Pancreatic Surgery Department of the First Affiliated Hospital of Harbin Medical University; 2.Two weeks before taking medication, there was no antibiotic treatment and no severe diarrhea; 3.Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with severe acute pancreatitis; 2.There are serious intestinal diseases such as inflammatory bowel disease (Crohn's disease, ulcerative colitis), intestinal obstruction, intestinal perforation, intestinal cancer, intestinal ischemia, necrotizing enterocolitis and some serious infectious diseases; 3.Individuals with bacteremia, sepsis, and severe abdominal infections; 4.History of using antibiotics, acid suppressants, and other medications within two weeks; 5.Individuals over 65 years old with a high incidence of underlying diseases; 6.Combined with serious physical diseases or organic lesions in the brain, such as severe organ dysfunction of the heart, liver, and kidneys, malignant tumors, etc; 7.Those who are unable to collect feces; 8.Pregnant, perinatal, or lactating women.

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative complications related to pancreatic surgery;

Secondary

MeasureTime frame
Dynamic changes in inflammatory markers;Length of hospital stay and hospitalization costs;

Countries

China

Contacts

Public ContactSun Bei

The First Affiliated Hospital of Harbin Medical University

sunbei70@163.com+86 136 0365 6935

Outcome results

None listed

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