Preoperative Optimisation of Modifiable Risk Factors in Surgery of the Pancreas
Recruiting
N/A
Interventional Study
Prehabilitation
Pancreas Cancer
Surgery
Postoperative Complications
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 2,575 (estimated)
- Sponsor
- Maastricht University Medical Center · Other
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About This Trial
The goal of this stepped-wedge randomized controlled trial is to investigate whether implementation of a best practice program for preoperative optimisation (prehabilitation program) with a focus on screening, assessment, and intervention of 8 potentially (partly) modifiable risk factors in patients with (suspected) pancreatic cancer will improve outcome. The main questions it will aim to answer a…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* All patients who are planned for a curative treatment with or without neoadjuvant treatment and elective pancreatic resection in one of the centres of the Dutch Pancreatic Cancer Group (i.e. all centres performing major pancreatic surgery)
Exclusion Criteria:
* age \< 18 yea…
Contacts