MedPath

A randomised controlled single blinded multicentre trial of polyethylene glycol sealant to the staple line vs staple line alone in distal pancreatectomy.

Not Applicable
Conditions
Pancreatic Surgery
Surgery - Surgical techniques
Oral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
Registration Number
ACTRN12620001336976
Lead Sponsor
Institute for Breathing and Sleep
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
80
Inclusion Criteria

•18 years and over
•Disease of the pancreatic body or tail with planned treatment with elective distal pancreatectomy
•Planned open or minimally invasive approach
•Participant able to provide informed consent
•Intraoperative completion of a distal pancreatectomy (with or without splenectomy)

Exclusion Criteria

•Participation in another trial that might alter the outcome measures of this trial
•Pre or intraoperative signs of obstruction of the pancreatic duct at the head of the gland
•Unable to provide informed consent or expected lack of compliance with postoperative regime
•Distal pancreatic resection with a staple not feasible
•Documented allergy to human serum albumin
•Renal dysfunction (eGFR <35)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath