Skip to content

Role of rifaximin in reducing infectious complications in acute pancreatitis

A randomized study to investigate role of rifaximin compared to standard of care in reducing infectious complications in acute pancreatitis - RICAP

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/07/043978
Enrollment
180
Registered
2022-07-13
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Health Condition 1: K859- Acute pancreatitis, unspecified

Interventions

Intervention1: Rifaximin: Rifaximin, 400 mg thrice daily, enteral route, Tablet/syrup, maximum upto 28 days. Control Intervention1: standard of care: standard of care

Sponsors

Anurag Kumar Tiwari
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged 18 years to 65 years presenting with their first attack of acute pancreatitis within first 14 days from onset of pancreatitis and have systemic inflammatory response syndrome (SIRS) at presentation will be included in the study.

Exclusion criteria

Exclusion criteria: Patients with previous history of pancreatic disease, evidence of active infection at presentation, presence of co-morbid malignancy, presence of obesity [BMI >35kg/msq] and not giving consent for study will be excluded.

Design outcomes

Primary

MeasureTime frame
1.Development of pancreatic/extrapancreatic infection or sepsis within 30 days from onset. 2.Development of new onset organ failure [By Sequential organ failure assessment (SOFA) score] after randomization Timepoint: 4 weeks

Secondary

MeasureTime frame
1. Serum levels of IL-6 at baseline and at 5 days after randomization in severe and moderately severe forms of pancreatitis. 2. Duration of hospitalization. Timepoint: 4 weeks

Countries

India

Contacts

Public Contactanurag kumar tiwari

Institute of medical sciences, Banaras Hindu University

tiwarianuragk@gmail.com7800322490

Outcome results

None listed

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