Skip to content

Effect of Saccharomyces boulardii on systemic inflammatory response syndrome in acute pancreatitis: a randomized controlled trial

Effect of Saccharomyces boulardii on systemic inflammatory response syndrome in acute pancreatitis: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075625
Enrollment
Unknown
Registered
2023-09-11
Start date
2023-09-11
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

Acute pancreatitis

Interventions

Saccharomyces boulardii group:Saccharomyces boulardii, orally, 2 sachets BID.
Routine therapy group:Routine therapy group

Sponsors

The First Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Diagnosis of acute pancreatitis; (2) SIRS score = 2 points (3) Within 72 hours of acute pancreatitis; (4) Be aged 18-75; 5. Be willing to follow the research procedure and sign the informed consent form

Exclusion criteria

Exclusion criteria: (1) Multiple organ failure (respiratory failure, circulatory failure, renal failure and intestinal failure) within 72 hours of onset; (2) Application of probiotics in the past 1 month; (3) Have metastatic malignant tumors, autoimmune diseases (such as systemic lupus erythematosus, autoimmune pancreatitis, giant cell arteritis, rheumatoid arthritis) or chronic infectious diseases (including human immunodeficiency virus or tuberculosis); (4) pregnant and lactating women; (5) Gastrointestinal fistula, gastrointestinal obstruction and other serious gastrointestinal lesions; Patients with central venous catheterization; (6) Pancreatitis after endoscopic retrograde cholangiopancreatography and chronic pancreatitis; biliary pancreatitis with acute purulent cholangitis; 7. Hypersensitivity to Saccharomyces boulardii.

Design outcomes

Primary

MeasureTime frame
SIRS;WBC;

Secondary

MeasureTime frame
procalcitonin;Indicators of bowel function: improvement in abdominal pain, bloating, diarrhoea, vomiting, and bowel sounds, and resumption of voluntary bowel movements; C-reactive protein;neutrophil %;

Countries

China

Contacts

Public ContactZhu Yin

The First Affiliated Hospital of Nanchang University

zhuyin27@sina.com+86 139 7084 1464

Outcome results

None listed

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