Clinical Trials Directory

Trials / Completed

CompletedNCT00370110

Effects of Itopride on Gastric Motor and Sensory Functions in Healthy Volunteers

A Double-blind, Randomized, Placebo-controlled, Single Center, Parallel Group Study to Evaluate the Effects of Itopride (100 mg and 200 mg t.i.d.) on Gastric Motor and Sensory Functions in Healthy Volunteers

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
45 (actual)
Sponsor
Forest Laboratories · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Itopride is a new compound that is already marketed in Japan and in some countries of Eastern Europe under the name of Ganaton. It is used to treat symptoms associated with gastroparesis. Due to inadequate gastric emptying, these patients often have symptoms of bloating, nausea and vomiting following ingestion of a meal. This is a randomized, parallel group, two dose double blind, placebo-controlled study evaluating the effects of itopride (100 mg and 200 mg three times daily) and placebo on gastric motor and sensory functions in healthy volunteers.

Detailed description

In order to compare the effects of two itopride doses (100 mg and 200 mg three times daily) and placebo on gastric emptying and small bowel transit, gastric accommodation, and postprandial symptoms in female and male healthy volunteers, the following methods, which have been extensively used and validated in the laboratory, will be used: Scintigraphic gastric emptying of solids and small bowel transit; single photon emission computed tomography to measure gastric accommodation; and the nutrient drink test to measure maximum tolerated volume and postprandial symptoms. Based on data acquired using the same methods in the laboratory, the sample size of 15 subjects per group provides 80% power to detect an effect size of 16% in the primary endpoint of the study, that is a change in gastric volume (postprandial - fasting). This magnitude of change is considered clinically relevant.

Conditions

Interventions

TypeNameDescription
DRUGItopride 100 mg100 mg three times daily
OTHERPlacebo
DRUGItopride 200 mg200 mg three times daily

Timeline

Start date
2005-08-01
Primary completion
2005-11-01
Completion
2005-11-01
First posted
2006-08-30
Last updated
2017-02-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00370110. Inclusion in this directory is not an endorsement.