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

NCT ID: NCT00303264

Last Updated: 2012-03-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 48 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-05-31
• Study Completion Date: 2007-08-31

Brief 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

Dyspepsia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Interventions

dexloxiglumide

Intervention Type: DRUG

Nexium (esomeprazole)

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Be male or female, 18 to 75 years of age, inclusive.
• Must understand English and be able to follow the instructions about completing the diary and questionnaires.
• At the time of Screening, have pain and/or discomfort in your upper abdomen for at least one day each week in the last month.
• At the time of Screening, have at least one other symptom of FD for at least one day each week in the last month.

Exclusion Criteria

• Have a known hypersensitivity to dexloxiglumide, any PPI, or aluminum/magnesium-containing antacids
• Have a history of organic diseases, structural or biochemical, of the gastrointestinal system that can cause dyspepsia.
• Have active irritable bowel syndrome (C-IBS, alt-IBS, D-IBS).
• Have findings leading to a clinical suspicion of other secondary causes of dyspepsia, including endocrine, metabolic and neurological disorders.
• Have a body mass (BMI) value of greater than 38 (applies to both males and females).
• Have been enrolled in a previous investigational study of dexloxiglumide.
• Have received treatment with any investigational drug within a 30-day period, or 5 half-lives, whichever is longer, prior to study entry.
• Use or dependence on "prohibited" medications at study entry.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Forest Laboratories

INDUSTRY

Sponsor Role: lead

Locations

For information regarding investigative sites please contact Forest Professional Affairs

St Louis, Missouri, United States

Countries

United States

Other Identifiers

DEX-MD-20

Identifier Type: -

Identifier Source: org_study_id