drugset / Trial / NCT06297954

Usefulness of Metoclopramide to Improve Endoscopic Visualization in Upper Gastrointestinal Bleeding

NCT06297954

Phase 3 Completed 50 enrolled Autonomous University of Nuevo León
RandomizedParallel-groupDouble-blindDiagnostic

Summary

A prospective, randomized, double-blind study will be conducted, including all patients with upper gastrointestinal bleeding, defined as vomiting blood or black bowel movements, within 24 hours prior to admission. Patients will be randomized to receive intravenous metoclopramide 20 mg or placebo, a placebo is a look-alike substance that contains no active drug. Then endoscopy will be performed in the following 120 minutes, evaluating endoscopic visualization with the modified Avgerinos scale.

Timeline

Start
2023-03-01
Primary completion
2024-06-01
Completion
2024-06-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Metoclopramide Small molecule 20 mg Intravenous

Indications

No indication recorded.