- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05291923
Predictors of Severity of Postoperative Pancreatic Fistula After Pancreatoduodenectomy
Predictors of Severity of Postoperative Pancreatic Fistula After Pancreatoduodenectomy.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
(a) Aim and Objective - The aim of this study is to evaluate the biochemical parameters and imaging findings as predictors of the severity of postoperative pancreatic fistula after pancreatoduodenectomy in early postoperative period
Methodology:
- Study population: All those operated for pancreatoduodenectomy during the period of December 2021 to May 2023 will be enrolled in this study, meeting the inclusion and exclusion criteria. On an average 3-4 cases are operated per month in ILBS.
- Study design: Prospective observational study.
- Study period: From the date of clearance by the Institutional Ethics Committee, till May 2023.
- Sample size with justification: All consecutive patients undergoing pancreatoduodenectomy for the above-mentioned study period (expected sample size 40)
- Intervention: none.
- Monitoring and assessment:
1) Definitions: International study group on pancreatic fistula definition of Post-Operative Pancreatic Fistula POPF) will be used which are as follows: drain output of any measurable volume of fluid on or after postoperative day 3 with an amylase content greater than 3 times the serum amylase activity
Variables to be assessed:
Patient characteristics - Age, Sex, Height, Weight, BMI, Serum albumin levels, Pancreatic parenchymal thickness- at spleno-portal confluence, Indication of Pancreatoduodenectomy -Peri ampullary mass, head of pancreatic mass, distal cholangiocarcinoma Operative Parameters - Duration of surgery, Blood Loss, Pancreatic consistency, Intraoperative remnant pancreatic parenchymal thickness at pancreatojejunostomy site/ spleno portal confluence.
Postoperative measurements -
- Drain Fluid amylase (POD 1,3 & 5) & serum amylase
- Serum Procalcitonin, C-reactive protein and albumin (POD 5)
- Remnant pancreatic parenchymal thickness & change in thickness at pancreaticojejunostomy site/splenoportal confluence on NCCT abdomen (POD 5)
- Presence & location of intra-abdominal collection by NCCT abdomen (POD 5)
- Interventions required if any for management of complications
Statistical Analysis: Data will be entered into Excel Worksheet and statistical analyses will be performed by SPSS Statistics version 22 (IBM Corp., Armonk, NY). Statistical data will be represented as frequencies (%) where the continuous variables will be expressed as medians and interquartile range (IQR). Continuous variables will be compared with the student t test and Mann-Whitney test as appropriate. Differences between proportions derived from categorical data will be compared with Chi-square or Fischer's exact test. Variables will be correlated with clinical outcomes. ROC curve will be used for biochemical markers and imaging findings Repeated analyses of measures will be applied wherever applicable.
Adverse effects: None
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Delhi
-
New Delhi, Delhi, India, 110070
- Institute of Liver and Biliary Sciences
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Consecutive patients undergoing Pancreatoduodenectomy at ILBS
- Duct to mucosa pancreaticojejunostomy
Exclusion Criteria:
- Refused for consent
- Age < 18 yrs
- Hepatopancreatoduodenectomy
- Multi-visceral resection
- Re-exploration before POD 5
- Pancreaticogastrostomy
- Dunking type of pancreaticojejunostomy
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Post whipple's procedure patients
|
no intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
change in pancreatic parenchymal thickness at pancreaticojejunostomy site/spleno-portal confluence on postoperative day 5 predicts the severity of postoperative pancreatic fistula after pancreatoduodenectomy in early postoperative period
Time Frame: Post operative day 5
|
Post operative day 5
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Levels of C-reactive protein among the different grades of post operative pancreatic fistula
Time Frame: Post operative day 5
|
Post operative day 5
|
|
Levels of serum albumin among the different grades of postoperative pancreatic fistula.
Time Frame: Post operative day 5
|
Post operative day 5
|
|
Levels of serum procalcitonin among the different grades of postoperative pancreatic fistula.
Time Frame: Post operative day 5
|
Post operative day 5
|
|
Intra-abdominal collection among the different grades of postoperative pancreatic fistula by NCCT abdomen.
Time Frame: Post operative day 5
|
Post operative day 5
|
|
Location of intra-abdominal collection among the different grades of postoperative pancreatic fistula by NCCT abdomen.
Time Frame: Post operative day 5
|
Post operative day 5
|
Collaborators and Investigators
Investigators
- Study Director: Dr Piyush Kumar Sinha, MCh, Institute of Liver and Biliary Sciences, New Delhi
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ILBS-POPF-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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