MedPath

Comparison of different methods for treatment of pseudocyst of pancreas

Not Applicable
Completed
Conditions
Health Condition 1: null- ASA 1/2 patients with pseudocyst of pancreas following acute pancreatitis
Registration Number
CTRI/2012/09/002969
Lead Sponsor
Indian Council of Medical research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

Symptomatic patients, with pseudocyst of size more than 6 cm and more than 6 weeks after an attack of acute pancreatitis, were included in the study

Exclusion Criteria

•Patients with chronic pancreatitis associated pseudocyst

•Patients who have undergone any form of intervention previously

•Patients with significant co-morbidities

•Patients unfit for general anesthesia

•Bleeding disorders

•Patients refusing consent

•Patients having significant necrotic debris not considered fit for endoscopic drainage. The presence of necrotic debris was assessed by ultrasound of the abdomen and if required magnetic resonance imaging. The volume of the cyst and that of necrotic debris was calculated and significant debris was defined as 30 % of debris volume/volume

•Presence of a pseudoaneurysm

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
â?¢Primary success rate was defined as cyst resolution by the intended modality after the index intervention within 4 weeks of interventionTimepoint: 4 weeks
Secondary Outcome Measures
NameTimeMethod
Complications requiring prolonged stay and /or repeat procedure <br/ ><br>Recurrence rates during a follow up of 3 months <br/ ><br>Conversion to the other mode of drainageTimepoint: 7 days, 6 weeks, 3 months
© Copyright 2025. All Rights Reserved by MedPath