Viewing Study NCT00261300



Ignite Creation Date: 2024-05-05 @ 12:10 PM
Last Modification Date: 2024-10-26 @ 9:21 AM
Study NCT ID: NCT00261300
Status: COMPLETED
Last Update Posted: 2012-05-07
First Post: 2005-12-02

Brief Title: Long-term Pantoprazole Trial in Patients With Symptoms of Chronic Acid Peptic Complaints BY1023VMG-708
Sponsor: Takeda
Organization: Takeda

Study Overview

Official Title: Long-term Pantoprazole Trial in Patients With Symptoms of Chronic Acid Peptic Complaints
Status: COMPLETED
Status Verified Date: 2008-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None