Reduced Pancreatic Fistula Rate Following Pancreaticoduodenectomy: Trial on Pancreaticogastrostomy Versus Pancreaticojejunostomy
|ClinicalTrials.gov Identifier: NCT00830778|
Recruitment Status : Completed
First Posted : January 28, 2009
Last Update Posted : September 12, 2012
The incidence of complications after pancreaticoduodenectomy (PD) is around 50 %. The postoperative course after PD is strongly dependent of the occurrence of pancreatic fistula (POPF), which determines postoperative mortality, length of hospital stay and costs. The incidence of POPF after PD is dependent of its definition, and is reported in up to 20% of patients.
There is disagreement on whether to perform a pancreaticojejunostomy (PJ) or a pancreaticogastrostomy (PG) after PD. The aim of the current randomized controlled trial is to study whether PG significantly reduces the rate of POPF following PD for pancreatic or peri-ampullary tumours. Secondary endpoints are the reduction of overall postoperative complication rate and their severity.
|Condition or disease||Intervention/treatment||Phase|
|Tumors||Procedure: Pancreaticojejunostomy Procedure: Pancreaticogastrostomy||Phase 3|
Hide Detailed Description
- Surgeons who have performed a minimum of five (5) PG and PJ procedures can include patients in this randomized trial.
- Any dissection device or technique is allowed.
Pancreatic anastomosis (PG or PJ)
- 1-layer or 2-layer anastomosis is allowed but has to be registered
- mono-filament and/or poly-filament suture material is allowed but has to be registered
- no pancreatic stent will be placed
- Drainage: one (1) or more closed drain(s) with or without suction is allowed in the vicinity of the pancreatic anastomosis
- Enteral tube feeding (tube positioned in the jejunum at the time of surgery, and distal to the pancreatic anastomosis) as well as total parenteral nutrition (TPN) is allowed
- Gastrostomy tube (percutaneous) is allowed
- Somatostatin: start intra-operatively and administered for seven (7) days after surgery at a dose of 6 mg/d
- Prophylactic use of antibiotics during 24h post-operatively
- Prophylactic use of Ranitidine as well as any PPI (proton pump inhibitor) is allowed to prevent peptic ulcer
Clinical evaluation and assessment criteria
- The number and type of POPF will be recorded according to the ISGPF guidelines and based on findings on day 3 (three) after surgery
- The number and type of postoperative complications will be recorded. The therapy-oriented severity grading system (TOSGS) of complications will be used and complications will be allocated to surgical (SSC) and non-surgical site (NSSC) complications
- The adequacy of the surgical resection margins (pR0) and the magnitude of the tumour-free resection margin (millimetres) will be monitored
- Postoperative length of hospital stay (LOS) will be registered
Patient randomization and registration procedure (randomization lists attached)
- This is a multicentric randomized controlled trial.
- Patient randomization will be done intra-operatively since a substantial number of patients could be dropped out intra-operatively because of the presence of unexpected intra-abdominal metastases at the time of surgery.
- Patient stratification will be performed for each centre and will be based on the diameter of the pancreatic duct. A pancreatic duct at the level of the surgical transsection margin measuring 3 millimetres or less in diameter is defined as being a "soft pancreas". A pancreatic duct measuring more than 3 millimetres is defined as a "hard pancreas".
- A prospective registration of following parameters will be performed: intra-operative diameter of the pancreatic duct at the surgical transection margin, diameter of the pancreas at the surgical transection margin, pancreatic tissue consistency assessed by the surgeon: soft vs. hard, post-operative pathology parameters.
Statistical analysis and sample size calculation based on a stratified design
- 40% of patients are expected to have a hard pancreas and 60% a soft pancreas.
- It is assumed that the magnitude of the effect of the intervention (PJ vs. PG) on the POPF rate, expressed as an odds ratio (OR), is similar in both strata.
- The needed sample size is calculated to have 80% power to detect a common odds ratio of 2.7. POPF rates of 12% and 20% are assumed after PJ within the hard and soft pancreas stratum respectively (yielding 4.8% and 8.4% after PG). Note that, given the unequal size strata, this leads to an expected POPF rate of 16.8% after PJ and 7% after PG (≈12% POPF overall).
- A 2-sided (with alpha=5%) Mantel-Haenszel test of OR=1 for stratified 2x2 tables is planned
- 168 patients are required per group (total patient population 336)
- Expected duration of recruitment: 3-4 years
- An interim analysis will be performed annually (i.e. after inclusion of 1/3 and 2/3 of the patients) to to allow early stop of the study (or accrual of patients in a specific treatment group) due to rejection of the null hypothesis. Using the O'Brien-Fleming method (O'Brien and Fleming 1979) results in respectively |3.471|, |2.454| and |2.004| as critical values for the Z-statistic at the three analysis moments. Otherwise stated, p-values are declared significant if <.00052, <0.0141 and <0.0451 at respectively the first interim analysis, the second interim analysis and at the final analysis.
- Exact 95% confidence intervals will be calculated for the POPF and post-operative complication rates within each stratum. A stratified Mann-Whitney U test will be used for the TOSGS grading.
Translational research: optional Prognostic relevance of gene expression profiling in pancreatic cancer: analyses will be performed at UZ.Leuven/KU.Leuven (project coordinator B.Topal)
- Fresh tissue samples from pancreatic cancer and from non-tumoral pancreatic tissue will be stored in RNA-later (samples in 2 separate tubes; 5-10 volumes of RNA-later)
- Sample tubes will be transported (or picked up by the coördinator's research team), within 3 days from sampling, to be stored in -80°C for further analyses
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||336 participants|
|Official Title:||Reduced Postoperative Pancreatic Fistula Rate Following Pancreaticoduodenectomy; Multicentric Randomized Controlled Trial on Pancreaticogastrostomy vs. Pancreaticojejunostomy|
|Study Start Date :||June 2009|
|Actual Primary Completion Date :||August 2012|
|Actual Study Completion Date :||September 2012|
Experimental: PG anastomosis
Pancreaticogastrostomy (PG) reconstruction/anastomosis after pancreaticoduodenectomy (PD)
Pancreaticogastrostomy (PG) reconstruction/anastomosis
Active Comparator: PJ anastomosis
Pancreaticojejunostomy (PJ) reconstruction/anastomosis after pancreaticoduodenectomy (PD)
Pancreaticojejunostomy (PJ) reconstruction/anastomosis
- Reduction of clinical postoperative pancreatic fistula (POPF) rate [ Time Frame: 3 years ]
- Reduction of overall postoperative pancreatic fistula rate [ Time Frame: 3 years ]
- Reduction of the severity of postoperative complications [ Time Frame: 3 years ]
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00830778
|University Hospital Gasthuisberg|
|Leuven, Belgium, 3000|
|Study Director:||Baki Topal, MD, PhD||Universitaire Ziekenhuizen Leuven|
|Principal Investigator:||Claude Bertrand, MD||Hospital Jolimont, Brussels|
|Principal Investigator:||Jean Closset, MD, PhD||Hospital Erasme (ULB), Brussels|
|Principal Investigator:||Henk Thieren, MD||AZ. St.Lucas, Brugge|
|Principal Investigator:||Franky Vansteenkiste, MD||General Hospital Groeninge|
|Principal Investigator:||Jean-Francois Gigot, MD, PhD||Université Catholique de Louvain|
|Principal Investigator:||Joseph Weerts, MD||St.Joseph Hospital, Liège|
|Principal Investigator:||Geert Roeyen, MD||University Hospital Antwerp, Antwerp|
|Principal Investigator:||Marc Janssens, MD||J.Palfijn Hospital, Antwerp|
|Principal Investigator:||Tom Feryn, MD||St.Jan Hospital, Brugge|
|Principal Investigator:||Steven Pauli, MD||Monica Hospital, Deurne|