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The Efficacy of Pantoprazole Treatment in Patients With Functional Dyspepsia

B

Bezmialem Vakif University

Status and phase

Unknown
Phase 4

Conditions

Nonulcer Dyspepsia

Treatments

Drug: Folic Acid
Drug: Pantoprazol

Study type

Interventional

Funder types

Other

Identifiers

NCT01608750
B.30.2.BAV.0.05.05/331

Details and patient eligibility

About

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

Enrollment

200 estimated patients

Sex

All

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

200 participants in 2 patient groups, including a placebo group

pantoprazole
Experimental group
Treatment:
Drug: Pantoprazol
folic acid
Placebo Comparator group
Treatment:
Drug: Folic Acid

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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