Prophylactic EUS-guided Gastroenterostomy in Advanced Periampullary Cancers: a Multicenter Randomized Controlled Trial

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this randomized controlled trial is to investigate the effectiveness and safety of Prophylactic EUS-gastroenterostomy (ProEUS-GE) as a preventative approach for malignant gastric outlet obstruction (MGOO) in men and women aged 18 years or older diagnosed with periampullary cancer. The main question this study aims to answer is can ProEUS-GE effectively prevent the occurrence of MGOO in patients with periampullary cancer? Patients will be randomly assigned to one of two groups: Group 1 (ERCP alone) or Group 2 (ERCP + ProEUS-GE). The study will compare the outcomes between these groups to determine the effectiveness of ProEUS-GE in preventing MGOO. Researchers will compare Group 1 (ERCP alone) with Group 2 (ERCP + ProEUS-GE) to see if the addition of ProEUS-GE leads to a reduced occurrence of MGOO in patients with periampullary cancer. The primary endpoint is the rate of malignant gastric outlet obstruction.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
View:

• Radiological diagnosis of a periampullary cancer that is precluded from upfront surgical resection of curative intent due to advanced tumor stage. These include locally advanced or metastatic cancers of the pancreatic head, distal bile duct, duodenum, or ampulla. cancers.

• Elevated liver function tests requiring ERCP without evidence of MGOO of significant gastroparesis (see exclusion criterion #3 and #4)

• ECOG 0 or 1

• ASA\<4

• Provision of informed consent

Locations
Other Locations
Canada
Jewish General Hospital
NOT_YET_RECRUITING
Montreal
McGill University Health Center
RECRUITING
Montreal
St-Michael's Hospital (SMH)
NOT_YET_RECRUITING
Toronto
France
Hôpital Privé des Peupliers
NOT_YET_RECRUITING
Paris
India
Asian Institute of Gastroenterology
NOT_YET_RECRUITING
Hyderabad
Contact Information
Primary
Yen-I Chen, MD
yen-i.chen@mgcill.com
(514) 934-1934
Backup
Myriam Martel, MSc
myriam.martel@muhc.mcgill.ca
Time Frame
Start Date: 2024-04-09
Estimated Completion Date: 2027-08
Participants
Target number of participants: 110
Treatments
Active_comparator: ERCP alone
ERCP procedure alone and management of MGOO will be on a wait-and-see approach, using endoscopic interventions performed only if obstruction is clinically diagnosed
Experimental: ERCP + ProEUS-GE
ERCP with prophylactic eus-guided gastroenterostomy
Related Therapeutic Areas
Sponsors
Leads: McGill University Health Centre/Research Institute of the McGill University Health Centre
Collaborators: Jewish General Hospital, Unity Health Toronto

This content was sourced from clinicaltrials.gov