Clinical trial · NCT06801899 · RECRUITING · NA
ToPanc Trial: Survival After Total Versus Partial Pancreaticoduodenectomy for Adenocarcinoma of the Pancreatic Head, Distal Cholangiocarcinoma, and Ampullary Cancer
Sponsor: Insel Gruppe AG, University Hospital Bern
Summary
The goal of this clinical trial is to learn if total removal of the pancreas is a preferable alternative to partial removal in patients with cancer of the pancreatic head who are at high risk of pancreatic leakage. The main question it aims to answer is: Does total pancreas removal improve survival without reducing quality of life compared to partial removal? The only study specific procedures are the collection of 2 blood samples (7.5ml for each time point, preoperatively and during the hospitalisation) and the completion of the questionnaires.
Interventions
- Total pancreatectomy (TP) · PROCEDURE
The investigators perform TP in patients who undergo surgical resection of a malignant tumor in the pancreatic head.
- Partial pancreaticoduodenectomy (PD) · PROCEDURE
The investigators perform partial PD with anastomosis of the pancreas in patients who undergo surgical resection of a malignant tumor in the pancreatic head. This is the current standard procedure.
Published eligibility criteria
Verbatim from the registry. Only the site can decide how these apply to a specific patient.
Inclusion Criteria: * Adult patients (age ≥ 18 years) scheduled to undergo PD for highly suspected or histologically proven, resectable pancreatic ductal adenocarcinoma (PDAC), distal cholangiocarcinoma (DCC), and/or ampullary cancer (pancreaticobiliary type) * Suspected pancreas anastomosis at high-risk for development of a postoperative pancreatic fistula (POPF) (grade "D" according to Schuh et al. (29): Estimation by CT scan, MRI, and/or Endoscopic Ultrasound * Written informed consent Exclusion Criteria: * Duodenal carcinoma, ampullary cancer (intestinal type), neuroendocrine tumors, benign tumors, chronic pancreatitis * Medical conditions that do not allow appreciation of the nature, scope, and possible consequences of the trial as judged by the investigator * Pregnancy. A beta-Human Chorionic Gonadotropin (bHCG) pregnancy test must to be performed for women of child-bearing potential (defined as premenopausal women who have not undergone surgical sterilization) * Inability to follow the study procedures, e.g., due to psychological disorders, dementia, etc.
Sites (10)
- Department of General, Visceral and Transplantation Surgery, University Hospital Münster, Münster, Germany · RECRUITING
- Department of General and Visceral Surgery, University Hospital Ulm, Ulm, Germany · RECRUITING
- Department of General and Visceral Surgery, Kantonsspital Aarau, Aarau, Switzerland · RECRUITING
- Department of Surgery, Kantonsspital Baden, Baden, Switzerland · RECRUITING
- Department of Visceral Surgery, University Hospital Basel, Basel, Switzerland · RECRUITING
- Inselspital, Bern University Hospital, Bern, Switzerland · RECRUITING
- Department of Visceral Surgery, University Hospital Geneva, Geneva, Switzerland · RECRUITING
- Department of General, Visceral, Endocrine and Transplantation Surgery, Kantonsspital St. Gallen, Sankt Gallen, Switzerland · RECRUITING
- Department of Surgery, Stadtspital Triemli Zürich, Zurich, Switzerland · RECRUITING
- Department of Surgery and Transplantation, University Hospital Zürich, Zurich, Switzerland · RECRUITING
Not medical advice. Trial0 is a navigation service, not a medical provider. Nothing here is medical advice or a recommendation to pursue any treatment; eligibility matching is informational, based on published registry criteria, and only the trial site or treating clinician can determine actual eligibility. Decisions belong with the patient and their own doctors. Registry data refreshed at most hourly; last update posted 2026-08-12.