Surgery is required for the treatment of many pancreatic conditions, either malignant or benign. Mortality of pancreatic surgery can be up to 3% even in expert centers. Morbidity is high, postoperative pancreatic fistula (POPF) being the main postoperative complication. In its current definition (drain output of any measurable fluid \>= postoperative day 3 with amylase content \>3 times the serum amylase activity and with clinical consequence), the incidence of postoperative PF is between 15 and 30 %. Most POPF resolve spontaneously but when refractory POPF occurs, it may lead to severe complications. POPF severity is graded as follows: grade B in case of change in medical management: infection without organ failure, specific medication (total parenteral nutrition, somatostatin analogs, antibiotics), persistent drainage \> 3 weeks, angiographic procedure for bleeding, prolonged hospital stay; grade C in case of reoperation or PF-related organ failure or death. No specific prophylactic treatment of POPF is currently recommended by clinical guidelines. In clinical research, many prophylactic strategies have been attempted with partial efficacy. Endoscopic pancreatic sphincterotomy with plastic stent placement is effective in pre-and postoperative management of pancreatic fistula but with the need of a highly competent interventional endoscopist. Intrapapillary botulinum toxin injection is believed to induce relaxation of the pancreatic sphincter, leading to a " pharmacological " pancreatic sphincterotomy without any morbidity. A recent phase I/II prospective study has shown promising results in this indication, with no clinically relevant pancreatic fistula when botulinum toxin was injected. Based on this observation we hypothesize that intrapapillary botulinum toxin injection during an endoscopic procedure before surgery could be effective for the prevention of post-surgical pancreatic fistula
Surgery is required for the treatment of many pancreatic conditions, either malignant or benign. Mortality of pancreatic surgery can be up to 3% even in expert centers. Morbidity is high, postoperative pancreatic fistula (POPF) being the main postoperative complication. In its current definition (drain output of any measurable fluid \>= postoperative day 3 with amylase content \>3 times the serum amylase activity and with clinical consequence), the incidence of postoperative PF is between 15 and 30 %. Most POPF resolve spontaneously but when refractory POPF occurs, it may lead to severe complications. POPF severity is graded as follows: grade B in case of change in medical management: infection without organ failure, specific medication (total parenteral nutrition, somatostatin analogs, antibiotics), persistent drainage \> 3 weeks, angiographic procedure for bleeding, prolonged hospital stay; grade C in case of reoperation or PF-related organ failure or death. No specific prophylactic treatment of POPF is currently recommended by clinical guidelines. In clinical research, many prophylactic strategies have been attempted with partial efficacy. Endoscopic pancreatic sphincterotomy with plastic stent placement is effective in pre-and postoperative management of pancreatic fistula but with the need of a highly competent interventional endoscopist. Intrapapillary botulinum toxin injection is believed to induce relaxation of the pancreatic sphincter, leading to a " pharmacological " pancreatic sphincterotomy without any morbidity. A recent phase I/II prospective study has shown promising results in this indication, with no clinically relevant pancreatic fistula when botulinum toxin was injected. Based on this observation we hypothesize that intrapapillary botulinum toxin injection during an endoscopic procedure before surgery could be effective for the prevention of post-surgical pancreatic fistula This study will be a prospective, multicentric, phase III, superiority, controlled, randomized (1:1), open-label, clinical trial with two parallel arms (intrapapillary botulinum toxin versus standard care), using a PROBE (Prospective Randomized Open Blinded End-point) methodology. Patients with scheduled distal pancreatectomy for any indication Sources of funding for the trial : French Ministry supports this study by PHRC-N 2017. The botulinum toxin provides by MERZ France (producer of Xeomin)
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
460
injection of Botulinum toxin A 100 UI, single dose administration, in the major papilla, in the Oddi sphincter, during upper gastrointestinal endoscopy.
PRAT
Clichy, France
RECRUITINGnumber of postoperative pancreatic fistula
Clinically relevant POPF (grade B and C) in the 3 months after Distal Pancreatectomy
Time frame: 3 months
number of postoperative pancreatic fistulas grade B
Grade of postoperative pancreatic fistulas B based on the ISGPF 2016 update
Time frame: 3 months
number of postoperative pancreatic fistulas grade C
Grade of postoperative pancreatic fistulas C based on the ISGPF 2016 update
Time frame: 3 months
Quantity of Biochemical leak after surgery
Biochemical leak after surgery
Time frame: 3 months
number of Postoperative complications
Postoperative complications : * intra-abdominal fluid collection * delayed gastric emptying * hemorrhage * pancreatitis * wound infection * other infectious complication
Time frame: 3 months
CLAVIEN-DINDO classification for post-surgical morbidity
CLAVIEN-DINDO classification for post-surgical morbidity
Time frame: 3 months
Number of hospital days
Health economics endpoints : duration of hospital stay
Time frame: 3 months
Number of hospital readmissions
Health economics endpoints : hospital readmissions
Time frame: 3 months
Number of transfer to intensive care unit and the duration of these stays
Health economics endpoints : transfer to intensive care unit and the duration of these stays
Time frame: 3 months
Number of fistularelated postoperative invasive procedures
Health economics endpoints : fistularelated postoperative invasive procedures
Time frame: 3 months
overall costs of hospitalization
Health economics endpoints : overall costs
Time frame: 3 months
Quality of life EQ-5D-5L questionnaire
The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1-digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state : LEVEL 1: indicating no problem LEVEL 2: indicating slight problems LEVEL 3: indicating moderate problems LEVEL 4: indicating severe problems LEVEL 5: indicating unable to/extreme problems
Time frame: 3 months
Number of sides effects (complications) related to the endoscopic botulinum toxin injection
number of sides effects (complications) related to the endoscopic botulinum toxin injection
Time frame: 3 months
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