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Gut decontamination by rifaximin in patients with predicted severe acute pancreatitis

Not Applicable
Conditions
Health Condition 1: K858- Other acute pancreatitis
Registration Number
CTRI/2021/11/037721
Lead Sponsor
Department of gastroenterology and heaptology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients with a diagnosis of Predicted acute pancreatitis as per Atlanta classification presenting within seven days of pain onset

Patients with a diagnosis of Predicted acute pancreatitis as per Atlanta classification presenting within seven days of pain onset

Age >18 years

With one of the following:

1.Predicted Severe acute pancreatitis indicated by 3 or more points according to Imrie score

2.Atlanta classifification

3.and/or CECT Abdomen findings of Balthazar grade D or E

Exclusion Criteria

1.Previous history of allergy to Rifaximin

2.Patient with pancreatic malignancy

3.Postoperative pancreatitis after pancreatic surgery Bacteriologically proved infected necrosis at the time of randomization

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Development of infection of pancreatic necrosis documented by : <br/ ><br>â?¢Presence of gas on CECT or <br/ ><br>â?¢by positive culture from fine needle aspiration(FNA) in peri-pancreatic collection or <br/ ><br>â?¢Clinical deterioration or fever(38.5oC or 100.3oF) in absence of other explainable cause of infection (ie Pulmonary, UTI or Line infections) <br/ ><br>2. Mortality <br/ ><br>Timepoint: 1.Time of discharge <br/ ><br>2.till 12 weeks <br/ ><br> <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
1.Duration of ICU or Hospital stay <br/ ><br>2.Development of organ failure <br/ ><br>Timepoint: 1. At discharge
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