Monitoring of patIents With Microdialysis Following Pancreaticoduodenectomy (MINIMUM)
Pancreatic Cancer, Pancreatic Neoplasms, Biliary Tract Cancer
About this trial
This is an interventional diagnostic trial for Pancreatic Cancer focused on measuring Pancreaticoduodenectomy, Pancreatectomy, Anastomosis, Surgical
Eligibility Criteria
Inclusion Criteria:
- Patients must be scheduled for a pancreaticoduodenectomy
- Subject must be ≥ 18 years
- Able to give written signed informed consent
- Investigator's assessment that the patient is able to understand, comply and follow the instructions needed to successfully participate in this trial
Exclusion Criteria:
- Allergic to Voluven® (Fresenius Kabi AS, Halden, Norway) and contrast given during CT scan
- Another study interfering with current study
- Pregnant
Sites / Locations
- Oslo University Hospital
Arms of the Study
Arm 1
Arm 2
Active Comparator
No Intervention
Patient with microdialysis
Patient without microdialysis
Intervention group - Patients will receive an intraperitoneal microdialysis catheter and will be monitored consecutively by microdialysis. The surgeon is familiar with the current microdialysis results at any time during the study period. The surgeon may intervene based on traditional symptoms and signs plus predetermined values of the microdialysis results.
The control group - The patients will not receive a microdialysis catheter. The patients are monitored according to current standards of care and the surgeon may intervene based only on traditional symptoms and signs.