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| Sponsor: | AstraZeneca |
|---|---|
| Information provided by: | AstraZeneca |
| ClinicalTrials.gov Identifier: | NCT00251914 |
Purpose
The aim is to evaluate if the resolution of upper abdominal symptoms (pain or burning) during an acid suppressive test trial of esomprazole given daily for 7 days predicts symptoms resolution at the end of a subsequent treatment period of 7 weeks.
| Condition | Intervention | Phase |
|---|---|---|
|
Gastrointestinal Disease Signs and Symptoms, Digestive Dyspepsia |
Drug: Esomeprazole |
Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study |
| Official Title: | Supportive Test for Acid-Related Symptoms (STARS I) With Esomeprazole and a Following 7-Week, Double-Blind, Randomized, Placebo Controlled Treatment Period in Subjects With Upper Gastrointestinal Symptoms and With Normal Findings at Esophagogastroduodenoscopy. |
| Estimated Enrollment: | 1500 |
| Study Start Date: | December 2002 |
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
Show 217 Study Locations| Study Director: | AstraZeneca Nexium Medical Sciences Director, MD | AstraZeneca |
More Information
| Study ID Numbers: | SD-NED-0021, D9610C00021 |
| Study First Received: | November 9, 2005 |
| Last Updated: | June 9, 2009 |
| ClinicalTrials.gov Identifier: | NCT00251914 History of Changes |
| Health Authority: | Italy: National Monitoring Centre for Clinical Trials - Ministry of Health |
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Signs and Symptoms Digestive System Diseases Molecular Mechanisms of Pharmacological Action Signs and Symptoms, Digestive Gastrointestinal Diseases Therapeutic Uses |
Anti-Ulcer Agents Gastrointestinal Agents Omeprazole Enzyme Inhibitors Dyspepsia Pharmacologic Actions |