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Symptom Assessment in Adult Patients With Erosive GERD (Gastroesophageal Reflux Disease) or enGERD (Endoscopic-Negative GERD) After Treatment With Pantoprazole (BY1023/M3-343)

2014-08-27 03:44:13 | BioPortfolio

Summary

The aim of this study is to compare investigator and patient-assessed gastroesophageal reflux disease symptoms in patients with erosive GERD or endoscopic-negative GERD (enGERD). An endoscopy will be performed at study start and study end. During the study, the patients will complete a patient-orientated, self-assessed reflux questionnaire (ReQuest™ questionnaire). The study duration consists of a baseline period (8 days) and treatment period (28 days). Pantoprazole (tablet) will be administered once daily at one dose level. The study will provide further data on safety and tolerability of pantoprazole.

Study Design

Allocation: Non-Randomized, Control: Uncontrolled, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Conditions

GERD

Intervention

Pantoprazole

Location

Altana Pharma/Nycomed
Bondi Junction
Australia
NSW 2022

Status

Completed

Source

ALTANA Pharma

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:44:13-0400

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Medical and Biotech [MESH] Definitions

None available.

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