Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07109180

Robot-assisted Versus Open Lateral Pancreaticojejunostomy for the Treatment of Symptomatic Chronic Pancreatitis (PANACOTTA)

Led by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Updated on 2025-08-07

28

Participants Needed

1

Research Sites

89 weeks

Total Duration

On this page

Sponsors

A

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Lead Sponsor

S

St. Antonius Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

PANACOTTA is a multicenter randomized controlled trial including patients with symptomatic chronic pancreatitis and a dilated main pancreatic duct to either robot-assisted or open lateral pancreaticojejunostomy. The PANACOTTA trial will assess the post-operative quality of recovery following robot-assisted versus open lateral pancreaticojejunostomy.

CONDITIONS

Official Title

Robot-assisted Versus Open Lateral Pancreaticojejunostomy for the Treatment of Symptomatic Chronic Pancreatitis (PANACOTTA)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • At least 18 years old
  • Indication for lateral pancreaticojejunostomy based on symptomatic chronic pancreatitis with morphine-dependent pain or at least 3 acute pancreatitis episodes per year
  • Dilated pancreatic duct of 5 mm or more with non-enlarged pancreatic head smaller than 40 mm
  • Confirmed chronic pancreatitis according to M-ANNHEIM diagnostic Criteria
  • Eligible for both robot-assisted and open surgical approaches
  • Provided written informed consent
Not Eligible

You will not qualify if you...

  • Suspected or confirmed current pancreatic cancer
  • ASA classification 4 or higher
  • Other painful conditions that make pancreatitis pain difficult to distinguish
  • Prior pancreatic surgery
  • Pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Amsterdam UMC

Amsterdam, Netherlands

Actively Recruiting

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Research Team

E

E. Kilinc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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