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Long-term Pantoprazole Trial in Patients With Symptoms of Chronic Acid Peptic Complaints (BY1023/VMG-708)

Primary Purpose

Gastroesophageal Reflux Disease (GERD), Peptic Ulcers

Status
Completed
Phase
Phase 3
Locations
Germany
Study Type
Interventional
Intervention
Pantoprazole
Sponsored by
Takeda
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastroesophageal Reflux Disease (GERD) focused on measuring Gastric acid, GERD, Gastroesophageal reflux disease, Pantoprazole, Proton pump inhibitor

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Main Inclusion Criteria: Patients who completed ALTANA Pharma study BY1023/FK3006 (long-term clinical trial regarding efficacy and tolerability of Pantoprazole in patients not responding to treatment with H2-receptor antagonists or omeprazole) Written informed consent Main Exclusion Criteria: Concomitant diseases Pregnant or nursing female patients; female patients of childbearing potential who are not using reliable contraception

Sites / Locations

  • Altana Pharma/Nycomed

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1

Arm Description

Pantoprazole 40 mg

Outcomes

Primary Outcome Measures

Safety (adverse events, laboratory values).

Secondary Outcome Measures

Evaluation of gastrointestinal symptoms, histological parameters.

Full Information

First Posted
December 2, 2005
Last Updated
May 4, 2012
Sponsor
Takeda
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1. Study Identification

Unique Protocol Identification Number
NCT00261300
Brief Title
Long-term Pantoprazole Trial in Patients With Symptoms of Chronic Acid Peptic Complaints (BY1023/VMG-708)
Official Title
Long-term Pantoprazole Trial in Patients With Symptoms of Chronic Acid Peptic Complaints
Study Type
Interventional

2. Study Status

Record Verification Date
December 2008
Overall Recruitment Status
Completed
Study Start Date
October 2000 (undefined)
Primary Completion Date
September 2007 (Actual)
Study Completion Date
July 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Takeda

4. Oversight

5. Study Description

Brief Summary
Gastroesophageal reflux disease (GERD) is a medical condition affecting the stomach and esophagus. GERD might occur when the lower esophageal sphincter does not close properly and stomach contents leaks back (refluxes) into the esophagus. GERD is one of the most common medical disorders, with estimates of up to 50% of adults reporting reflux symptoms. One of the main symptoms of GERD is heartburn. It occurs when the acidic content from the stomach touches the lining of the esophagus, causing a burning sensation in the chest or throat. Proton pump inhibitors such as pantoprazole can relieve symptoms of GERD and peptic ulcers in a large proportion of patients. Additionally, long-term treatment with proton pump inhibitors may be needed for patients with chronic ulcer disease not caused by H. pylori (H. pylori is a stomach-dwelling bacteria which is often associated with ulcers in the stomach or duodenum). The aim of the study is to evaluate the long-term effect of pantoprazole in patients with chronic gastric acid-related complaints. The study duration consists of a 5-year treatment period. Pantoprazole will be administered once daily. The study will provide further data on long-term safety, tolerability, and efficacy of pantoprazole.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastroesophageal Reflux Disease (GERD), Peptic Ulcers
Keywords
Gastric acid, GERD, Gastroesophageal reflux disease, Pantoprazole, Proton pump inhibitor

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Pantoprazole 40 mg
Intervention Type
Drug
Intervention Name(s)
Pantoprazole
Intervention Description
Long term Pantoprozole trial
Primary Outcome Measure Information:
Title
Safety (adverse events, laboratory values).
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Evaluation of gastrointestinal symptoms, histological parameters.
Time Frame
5 years

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Main Inclusion Criteria: Patients who completed ALTANA Pharma study BY1023/FK3006 (long-term clinical trial regarding efficacy and tolerability of Pantoprazole in patients not responding to treatment with H2-receptor antagonists or omeprazole) Written informed consent Main Exclusion Criteria: Concomitant diseases Pregnant or nursing female patients; female patients of childbearing potential who are not using reliable contraception
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gorig Brunner, Prof. Dr.
Organizational Affiliation
30659 Hannover, Germany
Official's Role
Principal Investigator
Facility Information:
Facility Name
Altana Pharma/Nycomed
City
Hannover
ZIP/Postal Code
30659
Country
Germany

12. IPD Sharing Statement

Learn more about this trial

Long-term Pantoprazole Trial in Patients With Symptoms of Chronic Acid Peptic Complaints (BY1023/VMG-708)

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