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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01527084
Other study ID # 8760PG11
Secondary ID
Status Completed
Phase N/A
First received January 21, 2012
Last updated November 8, 2014
Start date July 2011
Est. completion date December 2012

Study information

Verified date November 2014
Source Postgraduate Institute of Medical Education and Research
Contact n/a
Is FDA regulated No
Health authority India: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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


Description:

In present study we plan to determine the appropriate timing of surgical intervention after PCD in step up approach of Infected pancreatic necrosis (IPN).

The investigators also intend to evaluate the role of PCD in obviating the surgical intervention in the management of IPN and evaluate the risks & benefits of extended treatment policy of PCD in step up approach of IPN in comparison to early surgery after PCD.


Recruitment information / eligibility

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

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
surgical intervention after percutaneous catheter drainage
Patients who are not improving by day 10 after PCD insertion will be included in the present study and are randomized to group A (early surgery i.e. between 10-15days after PCD insertion ) or group B (Extended treatment with PCD with saline irrigation for more than 15days after PCD insertion)

Locations

Country Name City State
India PGIMER Chandigarh
India Postgraduate Institute of Medical Education and Research Chandigarh

Sponsors (1)

Lead Sponsor Collaborator
Postgraduate Institute of Medical Education and Research

Country where clinical trial is conducted

India, 

Outcome

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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