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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01215058
Other study ID # NIS-PFR-DUM-2010/2
Secondary ID
Status Withdrawn
Phase N/A
First received September 28, 2010
Last updated October 21, 2010
Start date October 2010
Est. completion date April 2011

Study information

Verified date October 2010
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority France: French Data Protection Authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to assess gastroprotective agent compliance in patients at risk suffering from a gastrointestinal bleeding ulcer or a symptomatic ulcer with NSAID.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date April 2011
Est. primary completion date April 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients at risk suffering from a gastrointestinal bleeding ulcer or a symptomatic ulcer confirmed by endoscopy

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Outcome

Type Measure Description Time frame Safety issue
Primary Gastroprotective agent compliance At the end of 1 month No
Secondary Clinical characteristics of those ulcers with NSAID At the end of 1 month No
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