A Phase II Trial of Lanreotide for the Prevention of Postoperative Pancreatic Fistula

PHASE2CompletedINTERVENTIONAL
Enrollment

114

Participants

Timeline

Start Date

February 20, 2018

Primary Completion Date

February 1, 2021

Study Completion Date

April 1, 2021

Conditions
Pancreatic LeakPancreatic FistulaPancreaticoduodenal; FistulaPancreatectomy; Hyperglycemia
Interventions
DRUG

Lanreotide Prefilled Syringe

All patients enrolled in this study will receive SOMATULINE DEPOT 120 mg immediately prior to planned pancreatic resection. The pharmacist will dispense loaded syringes of the study drug. The single preoperative dose will be given in the pre-surgical center at the University of Washington by a trained health care professional. The study drug will be injected via the deep subcutaneous route in the superior external quadrant of the buttock.

Trial Locations (1)

98195

University of Washington Medical Center, Seattle

All Listed Sponsors
lead

University of Washington

OTHER

NCT03174353 - A Phase II Trial of Lanreotide for the Prevention of Postoperative Pancreatic Fistula | Biotech Hunter | Biotech Hunter