Clinical trialNAUnknown
POstopeRative Standardization of Care: THe Implementation of Best Practice After Pancreatic Resection
POstopeRative Standardization of Care: THe Implementation of Best Practice After Pancreatic Resection. a Nationwide Stepped-Wedge Cluster Randomized Trial
- Outcome
- Outcome unknown
- Phase
- NA
- Status
- Unknown
- Study type
- Interventional
- Start
- 8 January 2018
- Expected end
- 9 February 2020
- Enrollment
- 1,600 participants
- Sites
- 17
- Primary outcomes
- Composite primary endpoint
- Sponsor
- Other
- Results posted
- No
- Last update
- 14 June 2019
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Brief summary public domain (ClinicalTrials.gov)
This Nationwide stepped-wedge cluster randomized trial is designed to evaluate if the implementation of a best practice algorithm for postoperative care results in a decrease in incidence of major complications and death after pancreatic resection as compared to current practice.
Detailed description public domain (ClinicalTrials.gov)
Rationale Pancreatic resection is a major abdominal operation with 50% chance of postoperative complications. A feared complication is severe pancreatic fistula, in which there is leakage of enzyme rich fluid into the abdominal cavity. Adequate complication management appears to be the most important factor in improving outcomes of patients undergoing pancreatic resection. Objective To investigate whether implementation of a best practice algorithm for postoperative care focusing on early detection and step-up management of postoperative pancreatic fistula results in a lower rate of major complications and death after pancreatic resection as compared to current practice Study design A nationwide stepped-wedge, cluster randomized, superiority trial. In this design all participating centers cross over from current practice to best practice according to the algorithm, but are randomized to determine the exact order. At the end of the trial, all centers will have implemented the best practice algorithm. Study population All centers performing pancreatic surgery in the Netherlands (i.e. the Dutch Pancreatic Cancer Group). Intervention Cluster level education on postoperative care according to a best practice algorithm, focusing on early detection and step-up management of postoperative pancreatic fistula. This algorithm is based on findings in Dutch observational cohort studies, systematic literature analyses, an inventory in current protocols on postoperative care and expert opinion. The proposed algorithm is validated in a multicenter cohort and consensus upon this algorithm is reached with pancreatic surgeons from all centers of the Dutch Pancreatic Cancer Group. The final algorithm was reviewed critically by the advisory committee of internationally respected experts in the field of pancreatology before implementation in this trial. Comparison Postoperative care according to current practice. Endpoints The primary outcome was measured in all patients undergoing pancreatic resection and is a composite of major complications (i.e. postpancreatectomy bleeding, new-onset organ failure and death). Secondary endpoints include the individual components of the primary endpoint and other clinical outcomes, number of patients receiving adjuvant chemotherapy, healthcare resource utilization and costs analysis. Follow-up will be 90 days after pancreatic resection.
Intervention public domain (ClinicalTrials.gov)
Other: Best practice algorithm for postoperative care. See arm/group description
Arm public domain (ClinicalTrials.gov)
Best practice (experimental): Postoperative care according to a best practice algorithm for postoperative care focussing on early detection and minimally invasive management of postoperative pancreatic fistula.
Arm public domain (ClinicalTrials.gov)
Current practice (no intervention): Postoperative care according to current usual practice.
Primary outcome public domain (ClinicalTrials.gov)
Composite primary endpoint. The primary endpoint of this trial is a composite of the most severe complications associated to postoperative pancreatic fistula. This endpoint will be considered positive if one of the following complications occurs within 90 days after pancreatic resection: late postpancreatectomy bleeding, new-onset organ failure and/or death Time frame: 90 days after index pancreatic resection.
Secondary outcome public domain (ClinicalTrials.gov)
Postoperative mortality. Time frame: 90 days after index pancreatic resection.
Secondary outcome public domain (ClinicalTrials.gov)
New-onset organ failure. Time frame: 90 days after index pancreatic resection.
Secondary outcome public domain (ClinicalTrials.gov)
Late postpancreatectomy bleeding. Time frame: 90 days after index pancreatic resection.
Secondary outcome public domain (ClinicalTrials.gov)
Postoperative morbidity. Time frame: 90 days after index pancreatic resection.
Secondary outcome public domain (ClinicalTrials.gov)
Adjuvant chemotherapy. Time frame: 90 days after index pancreatic resection.
Secondary outcome public domain (ClinicalTrials.gov)
Success of implementation. Time frame: 90 days after index pancreatic resection.
Eligibility public domain (ClinicalTrials.gov)
Inclusion Criteria for Clusters: * All Dutch centers performing pancreatic surgery (i.e. performing at least 20 pancreatoduodenectomies a year) Exclusion Criteria for Clusters: * None Inclusion Criteria for Patients: * Patients underoging pancreatic resection for any indication Exclusion Criteria for Patients: * None (i.e. complete enumeration)
Enrollment public domain (ClinicalTrials.gov)
Enrollment: 1600 participants (estimated).