Heartburn Clinical Trial
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 Heartburn
Verified date | February 2017 |
Source | Forest Laboratories |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to evaluate the effects of itopride in patients with heartburn.
Status | Completed |
Enrollment | 48 |
Est. completion date | December 2006 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Otherwise healthy males and females aged 18-70, with at least 3 episodes of heartburn or acid regurgitation per week. |
Country | Name | City | State |
---|---|---|---|
United States | The Oklahoma Foundation for Digestive Research | Oklahoma City | Oklahoma |
Lead Sponsor | Collaborator |
---|---|
Forest Laboratories |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 24-hour pH Monitoring | after 5 days of treatment |
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