GERD Clinical Trial
Official title:
A Prospective, Non Interventional Study to Evaluate the Effects on Quality of Life, Symptoms and Productivity in Patients With Gastroesophageal Reflux Disease (GERD) After 6 Weeks Structured Treatment in a Company Health Care Setting
Verified date | December 2010 |
Source | AstraZeneca |
Contact | n/a |
Is FDA regulated | No |
Health authority | Sweden: Regional Ethical Review Board |
Study type | Observational |
The study aims to evaluate if a GERD treatment programme, in accordance with current regional recommendations, in a company health care setting, has an impact on health related quality of life (HRQoL), symptoms, and productivity in GERD patients.
Status | Completed |
Enrollment | 36 |
Est. completion date | June 2009 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Female and/or male aged > 18 years - Diagnosis of GERD confirmed - Prescription of GERD treatment or already receiving GERD treatment Exclusion Criteria: - Any symptom suggesting a need for further investigation - Previous participation in the present study - Current participation in a clinical study or participation in a clinical study during the last 30 days |
Observational Model: Case-Only, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Sweden | Research Site | Hälsocenter | Södertälje |
Lead Sponsor | Collaborator |
---|---|
AstraZeneca |
Sweden,
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