Survey examining the frequency and severity of acid related symptoms while taking Nexium
Study identifier:NIS-GAL-NEX-2010/1
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Study Complete
Official Title
A National, Multicentre, Open-label, Non-comparative, Non-interventional survey examining the frequency and severity of acid related symptoms while taking Nexium
Medical condition
gastric acid suppression
Phase
-
Healthy volunteers
No
Study drug
-
Sex
All
Actual Enrollment
491
Study type
Observational
Age
18 Years +
Date
Study Start Date: 01 May 2010
Primary Completion Date: 01 Nov 2010
Study Completion Date: 01 Nov 2010
Study design
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verification:
Verified 01 Jan 2015 by AstraZeneca
Sponsors
AstraZeneca
Collaborators
-
Inclusion and exclusion criteria
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No locations available
| Arms | Assigned Interventions |
|---|---|
| 1 | - |
Contacts
Investigators
Principal Investigator
Karin Otter
Medical Director BBC
