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Clinical Trials/NCT01608750
NCT01608750
Unknown
Phase 4

The Efficacy of Pantoprazole Treatment in Patients With Functional Dyspepsia: Randomised, Double-blind, Placebo-controlled Trial.

Bezmialem Vakif University1 site in 1 country200 target enrollmentJune 2012

Overview

Phase
Phase 4
Intervention
Pantoprazol
Conditions
Nonulcer Dyspepsia
Sponsor
Bezmialem Vakif University
Enrollment
200
Locations
1
Primary Endpoint
Effectiveness of pantoprazole treatment in patients with functional dyspepsia measured by symptoms scale.
Last Updated
13 years ago

Overview

Brief Summary

The aim of our study is to evaluate the effectiveness of proton pump inhibitor (PPI) treatment in patients with functional dyspepsia.

Registry
clinicaltrials.gov
Start Date
June 2012
End Date
June 2013
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Birol Baysal

Gastroenterologist

Bezmialem Vakif University

Eligibility Criteria

Inclusion Criteria

  • aged 18-45 years with symptoms of dyspepsia,
  • no evidence of organic disease.

Exclusion Criteria

  • Patients with alarm symptoms,
  • Severe concomitant illness,
  • Pregnancy or lactation,
  • Alcohol or drug abuse,
  • Use of aspirin or other non-steroidal anti-inflammatory drugs antibiotics, H2 receptor blockers, bismuth, or proton pump inhibitors in the preceding two weeks

Arms & Interventions

pantoprazole

Intervention: Pantoprazol

folic acid

Intervention: Folic Acid

Outcomes

Primary Outcomes

Effectiveness of pantoprazole treatment in patients with functional dyspepsia measured by symptoms scale.

Time Frame: one year

Study Sites (1)

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