A Study to Assess the Efficacy, Safety and Tolerability of Tegaserod Alone and in Combination With Omeprazole Given Orally in Patients With Symptoms of Symptomatic Gastroesophageal Reflux Disease (sGERD)
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ClinicalTrials.gov Identifier: NCT00149851 |
Recruitment Status :
Completed
First Posted : September 8, 2005
Last Update Posted : September 1, 2010
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Symptomatic Gastroespohageal Reflux Disease | Drug: Tegaserod | Phase 2 |
Study Type : | Interventional (Clinical Trial) |
Enrollment : | 832 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Double |
Primary Purpose: | Treatment |
Official Title: | A Study to Assess the Efficacy, Safety and Tolerability of Tegaserod Alone and in Combination With Omeprazole Given Orally in Patients With Symptoms of Symptomatic Gastroesophageal Reflux Disease (sGERD) |
Study Start Date : | January 2004 |
Actual Primary Completion Date : | June 2005 |
Actual Study Completion Date : | June 2005 |

- Proportion of patients experiencing resolution of heart-burn during week 4 of treatment
- Proportion of patients experiencing resolution of heart-burn during week 4 of treatment in combination with Omeprazole and compared with Omeprazole alone
- Decreasing frequency of regurgitation during week 4 of treatment
- Decreasing frequency of regurgitation during week 4 of treatment in combination with Omeprazole and compared with Omeprazole alone

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Ages Eligible for Study: | 18 Years to 70 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Inclusion Criteria:
- History of physician diagnosed GERD
- Heartburn and Regurgitation 3 Days during the week prior to screening
Exclusion Criteria:
- History of erosive esophagitis, Barrett's esophagus, esophageal stricture, scleroderma, Zollinger-Ellison Syndrome, known primary disorder
- History or presence of infection or inflammation of the small or large intestine, gastrointestinal malignancy, history of upper GI surgery
- Use of PPI during the last four weeks prior to screening
Other protocol-defined inclusion/exclusion criteria may apply.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00149851
United States, New Jersey | |
Novartis | |
East Hanover, New Jersey, United States, 07936-108 |
Study Chair: | Novartis | East Hanover NJ |
ClinicalTrials.gov Identifier: | NCT00149851 |
Other Study ID Numbers: |
CHTF919B2203 |
First Posted: | September 8, 2005 Key Record Dates |
Last Update Posted: | September 1, 2010 |
Last Verified: | January 2008 |
GERD, heartburn, regurgitation, reflux disease |
Gastroesophageal Reflux Esophageal Motility Disorders Deglutition Disorders Esophageal Diseases Gastrointestinal Diseases Digestive System Diseases |
Tegaserod Serotonin Receptor Agonists Serotonin Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Physiological Effects of Drugs |