Clinical Trials Directory

Trials / Completed

CompletedNCT00303264

The Safety and Efficacy of Dexloxiglumide for the Relief of Symptoms of Functional Dyspepsia.

A Phase II Study to Investigate the Safety and Efficacy of Dexloxiglumide for the Relief of Symptoms of Functional Dyspepsia.

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
48 (actual)
Sponsor
Forest Laboratories · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

"Functional dyspepsia" has been defined loosely as "pain or discomfort centered in the upper abdomen." The symptoms can also include fullness, early satiety, bloating, belching, nausea, retching and vomiting. These symptoms may present with or without the co-existence of symptoms of heartburn or gastroesophageal reflux disease (GERD). Functional dyspepsia is a diagnosis of exclusion in which other disease states, such as ulcer, cancer, etc. are ruled out and the source of the pain is unknown. The standard of care for most patients presenting with dyspeptic symptoms has been with proton pump inhibitors (PPI), regardless of whether or not the patient's symptoms include acid-related conditions, e.g., heartburn, GERD, etc. Although PPI treatment has yielded some success in these patients, there is a significant population of patients whose dyspeptic symptoms are not adequately treated with PPI's alone. The purpose of this study is to evaluate the use of dexloxiglumide in the treatment of the symptoms of functional dyspepsia in patients whose dyspeptic symptoms are not being treated adequately with PPI's.

Conditions

Interventions

TypeNameDescription
DRUGdexloxiglumide
DRUGNexium (esomeprazole)

Timeline

Start date
2006-05-01
Primary completion
2007-08-01
Completion
2007-08-01
First posted
2006-03-16
Last updated
2012-03-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00303264. Inclusion in this directory is not an endorsement.