Pancreatic Cancer Clinical Trial
— REMBRANDTOfficial title:
The Effectiveness of Adding Braun Anastomosis to Standard Child Reconstruction to Reduce Delayed Gastric Emptying After Pancreatoduodenectomy (REMBRANDT): a Multicenter Randomized-controlled Trial
The goal of this clinical trial (REMBRANDT) is to evaluate the effectiveness of adding an extra connection (i.e. 'Braun anastomosis') after standard reconstruction in pancreatic head resection in reducing the incidence of delayed gastric emptying.
Status | Recruiting |
Enrollment | 256 |
Est. completion date | September 2025 |
Est. primary completion date | September 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Undergoing open pancreatoduodenectomy - Provided informed consent - Age over 18 years Exclusion Criteria: - Insufficient control of the Dutch language to read the patient information and to fill out the questionnaires in Dutch hospitals - Previous bariatric surgery (such as Roux-en-Y gastric bypass, gastric sleeve) - Pregnancy - Bowel motility disorders - Minimally invasive pancreatoduodenectomy - Gastric outlet syndrome |
Country | Name | City | State |
---|---|---|---|
Netherlands | Amsterdam UMC | Amsterdam | |
Netherlands | OLVG | Amsterdam | |
Netherlands | Catharina hospital | Eindhoven | |
Netherlands | Medical spectrum Twente | Enschede | |
Netherlands | Groningen UMC | Groningen | |
Netherlands | Medical center Leeuwarden | Leeuwarden | |
Netherlands | LUMC | Leiden | |
Netherlands | Maastricht UMC+ | Maastricht | |
Netherlands | St Antonius hospital | Nieuwegein | |
Netherlands | Radboud UMC | Nijmegen | |
Netherlands | Erasmus MC | Rotterdam | |
Netherlands | Isala hospital | Zwolle |
Lead Sponsor | Collaborator |
---|---|
Radboud University Medical Center | Rising Tide Foundation |
Netherlands,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Delayed gastric emptying (DGE) | DGE is defined by the need for maintenance of the nasogastric tube (NGT), need for reinsertion of NGT for persistent vomiting after postoperative day (POD) 7, or inability to tolerate a solid diet. | During hospitalization | |
Secondary | Pancreatic fistula (POPF) | Any measurable volume of drain output with an amylase level of more than 3 times the upper limit of normal serum amylase and clinically relevant condition or development of the patient directly related to the POPF. | During hospitalization | |
Secondary | Anastomotic leak | Anastomotic leaks of the hepatojejunostomy (HJ) or Braun enteroenterostomy (BE).
Anastomotic leaks of the HJ manifest as bile leakage. This is defined as "fluid with an increased bilirubin concentration in the abdominal drain or in the intra-abdominal fluid on or after postoperative day 3, or as the need for radiologic intervention because of biliary collections or relaparotomy resulting from bile peritonitis. Increased bilirubin in the drain is defined as bilirubin concentration more than 3 times greater than the serum bilirubin concentration. An anastomotic leak of the BE is present when an abdominal CT with contrast shows leakage of contrast from the BE or when during relaparotomy dehiscence of the BE is apparent. |
During hospitalization | |
Secondary | Postoperative complications: incidence and severity | Scored according to the modified Clavien-Dindo classification for surgical complications. Grade III and higher are considered clinically relevant in this study. | During hospitalization | |
Secondary | Number of days participants were hospitalized | The time period in days between hospital admission and discharge from the hospital. | During hospitalization | |
Secondary | Number of participants with in-hospital mortality | Any death during hospital admission. | During hospitalization | |
Secondary | 30-day mortality | Any death occurring 30 days after pancreatoduodenectomy. | 30 days | |
Secondary | Quality of life (QoL) based on five dimensions | The EQ-5D-5L standardized questionnaire will be used. | Change from baseline at 1 week, at 2 weeks, and 3 months | |
Secondary | Participants perceived disease and treatment related quality of life | The European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30/PAN26 standardized quality of life questionnaires will be used. | Change from baseline at 2 weeks, 3 months, and 12 months | |
Secondary | Quality of recovery | The QoR-15 standardized questionnaire will be used. | Change from baseline at 1 week, at 2 weeks, and 3 months | |
Secondary | Functional outcome at 12 months | Participants will be phoned to assess whether they have complaints of delayed gastric emptying ("afferent loop syndrome"). | 12 months |
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