Sponsor:
Medtronic - MITG
Code:
NCT06188585
Conditions
Acute Gastrointestinal Bleeding
Eligibility Criteria
Sex: All
Age: 22+
Healthy Volunteers: Not accepted
Interventions
UI-EWD
Conventional therapy
Brief summary:
Conditions
Acute Gastrointestinal Bleeding
Study ID
NCT06188585
Start date
Jun 21, 2024
Status verified date
Jun, 2026
Completion date
Sep, 2029
Anticipated
Primary completion date
Aug, 2029
Anticipated
Eligibility Criteria
Sex: All
Age: 22+
Healthy Volunteers: Not accepted
Enrollment
278 participants
Anticipated
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary purpose
Treatment
Arms
experimental: Test Group
active comparator: Control Group
Interventions
UI-EWD
Conventional therapy
Primary outcome measure
Central contacts
Locations
Yale
Recruiting
New Haven, Connecticut, United States, 06520
Principal Investigator:
Kenneth Hung, M.D.
RUSH University
Recruiting
Chicago, Illinois, United States, 60612
Principal Investigator:
Neal Mehta, M.D.
Brigham and Women's Hospital
Recruiting
Boston, Massachusetts, United States, 02115
Principal Investigator:
Linda Lee, MD
Rutgers University
Recruiting
Piscataway, New Jersey, United States, 08901
Principal Investigator:
Arvind Trindade, M.D.
Northwell Health
Recruiting
Manhasset, New York, United States, 11030
Principal Investigator:
Juan Bucobo, M.D.
NYU Langone
Recruiting
New York, New York, United States, 10016
Principal Investigator:
Melissa Debordeaux, M.D.
McGill University
Recruiting
Montreal, Quebec, Canada
Principal Investigator:
Yen-I Chen, M.D.
St. Michael's Hospital
Recruiting
Toronto, Canada
Principal Investigator:
Jeffrey Mosko, MD, MSc, FRCPC
Vancouver General Hospital
Recruiting
Vancouver, Canada
Principal Investigator:
Roberto Trasolini, MD
Sponsor
Medtronic - MITG
Last update posted
Jun 22, 2026
Last verified
Jun, 2026
Keywords
Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Medtronic - MITG on 2026-06-22.