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Efficacy of Pantoprazole 20/40 mg Once Daily (od) in Patients Older Than 12 Years Who Have Gastrointestinal Symptoms of Reflux Disease (PARADE)

N

Nycomed

Status

Completed

Conditions

Gastroesophageal Reflux Disease

Treatments

Drug: Pantoprazole

Study type

Observational

Funder types

Industry

Identifiers

NCT00829738
P2-9999-011-DE

Details and patient eligibility

About

The aim of this study was to evaluate the effect of 14 days treatment with Pantoprazole 40 mg and 20 mg on gastroesophageal reflux disease (GERD) related symptoms in a large patient population.

Enrollment

4,188 patients

Sex

All

Ages

12+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Main inclusion criteria:

  • Outpatients with gastroesophageal reflux disease (GERD)

Main exclusion criteria:

  • Criteria as defined in the Summary of Product Characteristics

Trial design

4,188 participants in 1 patient group

Group 1
Description:
All patients enrolled
Treatment:
Drug: Pantoprazole

Trial contacts and locations

717

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Data sourced from clinicaltrials.gov

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