No registrations found.
ID
Source
Brief title
Health condition
Pancreatic cancer
Sponsors and support
Intervention
Outcome measures
Primary outcome
To examine the feasibility and safety of preoperative endoscopic BOTOX® injection in the sphincter of Oddi.
Secondary outcome
To examine the effect of preoperative endoscopic BOTOX® injection in the sphincter of Oddi on the occurrence of postoperative pancreatic fistulas.
Background summary
Despite advances in surgical techniques, the occurrence of postoperative pancreatic fistula (POPF) is still a major cause of potentially severe and costly morbidity after distal pancreatectomy. Good quality evidence on how to prevent POPF is lacking. Existing interventions such as somatostatin analogues, varying surgical closure techniques, pre-operative duct stenting or percutaneous drains, do not work well or have too many complications/side effects. Pre-operative peri-ampullary injection of BOTOX® might reduce the incidence of POPF by decreasing intra-ductal pressure via relaxation of the sphincter of Oddi. In this study we will first analyze the safety and feasibility of peri-ampullar endoscopic BOTOX® injections in a small group of patients (n=15). If the procedure is safe and feasible we will continue this study in an additional 35 patients to investigate whether this procedure indeed reduces the POPF rate.
Study objective
Pre-operative peri-ampullary injection of BOTOX® might reduce the incidence of POPF by decreasing intra-ductal pressure via relaxation of the sphincter of Oddi.
Study design
Screening
Endoscopic BOTOX injection
Pancreatic surgery
2 weeks post surgery
4 weeks post surgery
Intervention
Pre-operative endoscopic BOTOX® injection. The single BOTOX® injection will consist of a 1 mL suspension of 100 units of BOTOX® reconstituted in 1 mL of 0.9% saline solution will be injected into the sphincter of Oddi (in the one o’clock position).
Inclusion criteria
• Age ≥ 18 years.
• Lesion(s) of the body and/or tail of the pancreas for which open, laparoscopic or robot-assisted distal pancreatectomy will be performed.
• Signed informed consent.
Exclusion criteria
• Hypersensitivity to BOTOX® (or the components in the BOTOX® formulation).
• American Society of Anesthesiologists score >III.
• Unable to undergo duodenoscopy (due to any anatomic condition).
• Pregnancy or lactation.
• Serious concomitant systemic disorders that would compromise the safety of the patient or his/her ability to complete the study, at the discretion of the investigator.
Design
Recruitment
IPD sharing statement
Followed up by the following (possibly more current) registration
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL8027 |
CCMO | NL68231.078.19 |
OMON | NL-OMON48251 |