Permanent plastic stenting in patients with pancreatic fluid collections and disconnected pancreatic duct syndrome: A randomized controlled study
Not Applicable
- Conditions
- Health Condition 1: K863- Pseudocyst of pancreas
- Registration Number
- CTRI/2020/07/026724
- Lead Sponsor
- Dr Surinder Rana Principal Invetsigator
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients of WON who have undergone EUS guided transmural drainage with metal stents
2.Patients having resolved WON and having DPDS on magnetic resonance cholangiopancreatography (MRCP)/Endoscopic retrograde cholangiopancreatography (ERCP)
3.Giving informed consent and willing to follow up regularly
Exclusion Criteria
1.Underlying chronic pancreatitis
2.Underlying pancreatic malignancy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary Outcome: <br/ ><br>1.Recurrence of Pancreatic Fluid collections <br/ ><br>2.Recurrence of abdominal pain <br/ ><br> <br/ ><br>Timepoint: Primary Endpoint: <br/ ><br>Proportion of patients with PFC recurrence at 12 months. <br/ ><br> <br/ ><br>Co-Primary Endpoint: <br/ ><br>Proportion of patients with recurrence of abdominal pain <br/ ><br>
- Secondary Outcome Measures
Name Time Method Secondary Outcome: <br/ ><br>1.Technical success of placement of plastic stent <br/ ><br>2.Adverse effects <br/ ><br>3.Stent Migration <br/ ><br>4.Diabetes Mellitus <br/ ><br>Timepoint: Base line <br/ ><br>3 months <br/ ><br>6 months <br/ ><br>12 months