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| Sponsor: | AstraZeneca |
|---|---|
| Information provided by: | AstraZeneca |
| ClinicalTrials.gov Identifier: | NCT00695838 |
Purpose
The purpose of this observational study is to assess the impact of abdominal fat on severity and frequency of GERD symptoms .
| Condition |
|---|
|
GERD |
| Study Type: | Observational |
| Study Design: | Cohort, Prospective |
| Official Title: | Evaluation of the Impact of Abdominal Fat on GERD Severity and GERD Frequency in General Practice |
| Enrollment: | 5084 |
| Study Start Date: | January 2008 |
| Study Completion Date: | December 2008 |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
First three consecutive patients with GERD symptoms seen by GP
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
Show 1638 Study Locations| Study Director: | Alain Castaigne, Medical Director | AstraZeneca |
More Information
| Responsible Party: | AstraZeneca Pharmaceuticals ( Alain Castaigne, Medical Director ) |
| Study ID Numbers: | NIS-GFR-DUM-2007/3 |
| Study First Received: | June 10, 2008 |
| Last Updated: | August 4, 2009 |
| ClinicalTrials.gov Identifier: | NCT00695838 History of Changes |
| Health Authority: | France: French Data Protection Authority |
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GERD symptoms- Waist circumference Patients with symptomatic GERD |
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Deglutition Disorders Esophageal Motility Disorders Digestive System Diseases |
Gastrointestinal Diseases Esophageal Diseases Gastroesophageal Reflux |