Intrapapillary Botulinum Toxin Injection for PREvention of Post-surgical PAncREactic Fistula

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

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

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with scheduled distal pancreatectomy for any indication: open or laparoscopic distal pancreatectomy with or without splenectomy

Age ≥ 18years

Disqualifiers

History of myasthenia gravis or Eaton-Lambert syndrome

Inflammatory myositis <2 years or preexisting motor neuron disease or neuropathies

ASA score > III

Pregnancy or lactation

Trial design

Design model

Parallel

Treatments tested in this trial

  • botulinum toxin injection

    Drug

    injection of Botulinum toxin A 100 UI, single dose administration, in the major papilla, in the Oddi sphincter, during upper gastrointestinal endoscopy.

Treatment groups

460 Participants
are divided into 2 treatment groups
Group A: botulinum toxin injectionExperimental treatment 1 intervention
Group B: standard careNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

number of postoperative pancreatic fistula

Clinically relevant POPF (grade B and C) in the 3 months after Distal Pancreatectomy

Time frame
3 months

Secondary outcomes

1

number of postoperative pancreatic fistulas grade B

Grade of postoperative pancreatic fistulas B based on the ISGPF 2016 update

Time frame
3 months
2

number of postoperative pancreatic fistulas grade C

Grade of postoperative pancreatic fistulas C based on the ISGPF 2016 update

Time frame
3 months
3

Quantity of Biochemical leak after surgery

Biochemical leak after surgery

Time frame
3 months
4

number of Postoperative complications

Postoperative complications : * intra-abdominal fluid collection * delayed gastric emptying * hemorrhage * pancreatitis * wound infection * other infectious complication

Time frame
3 months

Other outcomes

Sponsors and contacts

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