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The effect of proton pump inhibitors on acute pancreatitis--a randomly prospective control study

The effect of proton pump inhibitors on acute pancreatitis--a randomly prospective control study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-16008301
Enrollment
Unknown
Registered
2016-04-18
Start date
2016-04-11
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

acute pancreatitis

Interventions

experimental:esomeprazole 40mg/d
PPI-N group:conventional medical management
volunteers group:none

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed with acute pancreatitis; 2. The duration of the disease<= 72 hours (begin with the onset of abdominal pain); 3. Aged between 18 and 65 years old; 4. Sign informed consent.

Exclusion criteria

Exclusion criteria: 1. treatment with anti-acid agents or prokinetic drug during the past four weeks; 2. regular medicine treatment of antibiotics, NSAIDS, antidepressant, and immune suppression treatment; 3. history of enteroscopy during the past 1 month and history of chronic diarrhea, malabsorption, irritable bowel syndrome, inflammatory bowel disease; 4. organ failure, diabetes, thyroidea diseases, scleroderma and any other combined disease can influnce the intestinal mobility; 5. gastrointestinal operation and history of ileus; 6. Pregnant women and lactating women.

Design outcomes

Primary

MeasureTime frame
gastric pH;the prevalence of SIBO;change of gut microbiota;

Secondary

MeasureTime frame
index of inflammation;prevalence of infection;index of radioimmunity;modified CTSI;hospital stay;cost of hospitalization ;duodenum pH;prevalence of GI bleeding;APACHE II score;

Countries

China

Contacts

Public ContactChengwei Tang

Department of Gastroenterology, West China Hospital, Sichuan University

shcqcdmed@163.com+86 18980601275

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 17, 2026