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Comparison of Prilosec OTC® Versus Zegerid® for Gastric Acid Suppression

Procter & Gamble (P&G) logo

Procter & Gamble (P&G)

Status and phase

Completed
Phase 4

Conditions

Normal Healthy Subject Population

Treatments

Drug: Zegerid®
Drug: Prilosec OTC®

Study type

Interventional

Funder types

Industry

Identifiers

NCT00808769
2008122

Details and patient eligibility

About

The purpose of this study is to compare Prilosec OTC® and Zegerid® in their effects on gastric acid suppression.

Enrollment

30 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Normal subjects who are 18-65 years of age;
  • Non-childbearing potential females or those using birth control

Exclusion criteria

  • History of significant GI disease
  • Any significant medical illness
  • History of hypersensitivity, allergy or intolerance to omeprazole or other proton pump inhibitors;
  • Currently using GI medications
  • GI disorder or surgery leading to impaired drug absorption

Trial design

30 participants in 2 patient groups

1
Active Comparator group
Description:
Zegerid®
Treatment:
Drug: Zegerid®
2
Experimental group
Description:
Prilosec OTC®
Treatment:
Drug: Prilosec OTC®

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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