Acute Pancreatitis Clinical Trial
Official title:
Timing of Surgical Intervention After Percutaneous Catheter Drainage in STEP UP Approach for Severe Acute Pancreatitis: a Randomized Controlled Stud
1. To determine the appropriate timing of surgical intervention after Percutaneous
Catheter Drainage (PCD) in infected pancreatic necrosis (IPN).
2. To see the change in morbidity and mortality after changing the interval of surgery
after PCD
Status | Completed |
Enrollment | 40 |
Est. completion date | December 2012 |
Est. primary completion date | December 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 14 Years to 85 Years |
Eligibility |
Inclusion Criteria: - All patients with diagnosis of IPN (UK GUIDELINES) managed with percutaneous catheter drainage (PCD) for 10 to 15 days and not showing significant improvement on PCD will be included Exclusion Criteria: 1. Patient showing significant improvement on PCD within 10 days of its insertion.(Significant improvement on PCD is defined as resolution of fever, acceptance of enteral nutrition, decrease in total leukocyte count, reversal of organ system failure) 2. Sterile pancreatic necrosis 3. An acute intra abdominal event ( perforation of hollow viscus, bleeding, or the abdominal compartment syndrome) during or within 10 days after PCD insertion 4. Previous drainage or surgical necrosectomy for infected pancreatic necrosis (ERCP with or without papillotomy is allowed.) 5. Previous exploratory laparotomy for acute abdomen and diagnosis of pancreatitis during laparotomy |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
India | PGIMER | Chandigarh | |
India | Postgraduate Institute of Medical Education and Research | Chandigarh |
Lead Sponsor | Collaborator |
---|---|
Postgraduate Institute of Medical Education and Research |
India,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Mortality | participants will be followed for the duration of hospital stay, an expected average duration of 5 weeks | No | |
Primary | Reversal of existing organ failure | participants will be followed for the duration of hospital stay, an expected average duration of 5 weeks | No | |
Primary | New onset multiorgan failure or sepsis and systemic complications | participants will be followed for the duration of hospital stay, an expected average duration of 5 weeks | No | |
Primary | Locoregional complications | Pseudocyst, Pancreatic fistula, Enteric fistula, Perforation of a hollow viscus, and bleeding requiring intervention | participants will be followed for the duration of hospital stay, an expected average duration of 5 weeks | No |
Secondary | Proportion of patients in which surgery would be avoided in Group B | participants will be followed for the duration of hospital stay, an expected average duration of 5 weeks | No | |
Secondary | Pancreatic insufficiency (New onset Diabetes and steatorrhea) | participants will be followed for the duration of hospital discharge to end of our study period, an expected average duration of 1 year | No | |
Secondary | Total number of PCD catheters and catheter related interventions required, and catheter and drain related complications | participants will be followed for the duration of hospital stay, an expected average duration of 5 weeks | No |
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