Status:

COMPLETED

Nexium Capsules Clinical Experience Investigation

Lead Sponsor:

AstraZeneca

Conditions:

Gastric Ulcer, Duodenal Ulcer, Anastomotic Ulcer, Reflux Oesophagitis,"Non-erosive Reflux Disease, Zollinger-Ellison Syndrome

Eligibility:

All Genders

Brief Summary

The purpose of this study is to confirm the safety profile / factors which impact safety and efficacy of Nexium capsules in daily clinical usage for the patients who have been prescribed Nexium for "g...

Detailed Description

Nexium capsules Clinical Experience Investigation

Eligibility Criteria

Inclusion

  • Patients treated with Nexium for the first time due to gastric ulcer, duodenal ulcer, anastomotic ulcer, reflux oesophagitis, non-erosive reflux disease, Zollinger-Ellison syndrome.

Exclusion

  • None

Key Trial Info

Start Date :

September 1 2011

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

March 1 2014

Estimated Enrollment :

3691 Patients enrolled

Trial Details

Trial ID

NCT01434485

Start Date

September 1 2011

End Date

March 1 2014

Last Update

April 16 2014

Active Locations (47)

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Page 1 of 12 (47 locations)

1

Research Site

Aichi, Japan

2

Research Site

Akita, Japan

3

Research Site

Aomori, Japan

4

Research Site

Chiba, Japan