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Nexium Capsules Clinical Experience Investigation


N/A
N/A
N/A
Open (Enrolling)
Both
Gastric Ulcer, Duodenal Ulcer, Anastomotic Ulcer, Reflux Oesophagitis,"Non-erosive Reflux Disease, Zollinger-Ellison Syndrome

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Trial Information

Nexium Capsules Clinical Experience Investigation


Nexium capsules Clinical Experience Investigation


Inclusion Criteria:

- 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 Criteria: - None

Type of Study:

Observational

Study Design:

Observational Model: Cohort, Time Perspective: Prospective

Outcome Measure:

Number of Adverse Drug Reactions

Outcome Time Frame:

Patients with gastric ulcer, anastomotic ulcer or Zollinger-Ellison syndrome: 8 weeks

Safety Issue:

Yes

Principal Investigator

Shigeru Yoshida, MD

Investigator Role:

Study Director

Investigator Affiliation:

Astrazeneca K.K.

Authority:

Japan: Ministry of Health, Labor and Welfare

Study ID:

D961HC00010

NCT ID:

NCT01434485

Start Date:

September 2011

Completion Date:

December 2013

Related Keywords:

  • Gastric Ulcer, Duodenal Ulcer, Anastomotic Ulcer, Reflux Oesophagitis,"Non-erosive Reflux Disease, Zollinger-Ellison Syndrome
  • gastric ulcer, duodenal ulcer, anastomotic ulcer, reflux oesophagitis, non-erosive reflux disease, Zollinger-Ellison syndrome, Nexium
  • Duodenal Ulcer
  • Esophagitis
  • Esophagitis, Peptic
  • Gastroesophageal Reflux
  • Stomach Ulcer
  • Ulcer
  • Zollinger-Ellison Syndrome
  • Gastrinoma

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