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
| Type | Name | Description |
|---|---|---|
| DRUG | Pantoprazole | 40 mg pantoprazole once daily for 28 days |
| DRUG | Placebo | identical 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.