Clinical Trial: Efficacy and Safety of Itopride vs Placebo in Heartburn
Study Status: Completed
Recruit Status: Completed
Study Type: Interventional
Official Title: A Randomized, Double-blind, Two Period, Crossover Study to Evaluate the Effects of a Single Dose of Itopride 200 mg on Esophageal and Gastric pH and Reflux in Patients With Heart
Brief Summary: The purpose of this study is to evaluate the effects of itopride in patients with heartburn.
Detailed Summary:
Sponsor: Forest Laboratories
Current Primary Outcome: 24-hour pH Monitoring [ Time Frame: after 5 days of treatment ]
Original Primary Outcome:
Current Secondary Outcome:
Original Secondary Outcome:
Information By: Forest Laboratories
Dates:
Date Received: September 27, 2006
Date Started: October 2006
Date Completion:
Last Updated: February 7, 2017
Last Verified: February 2017