Clinical Trials Directory

Trials / Completed

CompletedNCT00915239

Symptom Evaluation After Cessation of a Proton Pump Inhibitor in Healthy Volunteers

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Sahlgrenska University Hospital · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine whether proton pump inhibitor (PPI) induced hypersecretion leads to acid related symptoms after treatment in healthy volunteers.

Detailed description

Treatment with proton pump inhibitors (PPI) has been shown to cause rebound hypersecretion of gastric acid. The clinical significance of this phenomenon is however unclear. This study aims to examine whether or not healthy volunteers, who over a relatively short period of time treated with a PPI, develop dyspeptic symptoms after cessation of therapy. Dyspeptic symptoms will be measured subjectively using a validated questionnaire, which is filled out each day. Gastric acid will be measured indirectly with measurement of acid secretion markers (Gastrin and chromogranin-A).

Conditions

Interventions

TypeNameDescription
DRUGPantoprazole40 mg pantoprazole once daily for 28 days
DRUGPlaceboidentical placebo once daily for 28 days

Timeline

Start date
2006-01-01
Primary completion
2006-10-01
Completion
2006-10-01
First posted
2009-06-05
Last updated
2009-06-05

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT00915239. Inclusion in this directory is not an endorsement.