CYP2C19 Genotype Predictor of Gastric Acid Suppression

Sponsor
Mayo Clinic (Other)
Overall Status
Withdrawn
CT.gov ID
NCT01824199
Collaborator
(none)
0
1
1
44.1
0

Study Details

Study Description

Brief Summary

If CYP2C19 genotype can predict the efficacy of healing erosive esophagitis and gastric acid secretion in patients taking once a day omeprazole.

Condition or Disease Intervention/Treatment Phase
Early Phase 1

Detailed Description

Proton pump inhibitors are metabolized through the CYP2C19 hepatic enzyme system. Several variant genotypes of this enzyme exist which may lead to decreased, normal or increased metabolism of the proton pump inhibitor. With alteration of metabolism, the degree of gastric acid suppression achieved and efficacy in treating reflux could be affected. For example, Asian populations who have low activity of CYP2C19, commonly need lower doses of proton pump inhibitors to manage gastroesophageal reflux because of more sustained blood levels and availability of the drug. Theoretically, those patients who are rapid metabolizers would receive less effective treatment with proton pump inhibitors

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
CYP2C19 Genotype as a Predictor of Gastric Acid Suppression and Healing of Erosive Esophagitis
Anticipated Study Start Date :
Mar 1, 2013
Actual Primary Completion Date :
Nov 1, 2016
Actual Study Completion Date :
Nov 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: Omeprazole

Patients will undergo whole blood testing for CYP2C19 genotype and will be started on omeprazole 40 mg once daily in the morning 30 minutes before breakfast. The Mayo Dysphasia Questionnaire 30 day (MDQ-30day) will be used during the study. At the end of 8 weeks, patients will undergo dual probe pH/impedance testing on therapy and a clinically indicated endoscopy to rule out Barrett's esophagus and assess healing. CYP2C19 genotyping will be performed in the Mayo laboratory.

Drug: Omeprazole
Patients with LA Grade B-D erosive esophagitis identified at the time of endoscopy will be prospectively recruited. Patients will undergo whole blood testing for CYP2C19 genotype and will be started on omeprazole 40 mg once daily in the morning 30 minutes before breakfast. The Mayo Dysphasia Questionnaire -30 day (MDQ-30day) will be used during the study. At the end of 8 weeks, patients will undergo dual probe pH/impedance testing on therapy and a clinically indicated endoscopy to rule out Barrett's esophagus and assess healing. CYP2C19 genotyping will be performed in the Mayo laboratory.
Other Names:
  • Prilosec
  • Outcome Measures

    Primary Outcome Measures

    1. The correlation specific to CYP2C19 genotype with gastric acid suppression by omeprazole. [8 weeks]

    Secondary Outcome Measures

    1. To assess patients gastrointestinal symptoms, in patients with EoE by means of standard validated questionnaires [30 days]

      trouble swallowing, heartburn, acid regurgitation

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion criteria:
    • Age 18 or older

    • Have either mild-to-moderate Los Angeles (LA) Classification System grade B, moderately severe LA grade C, or severe LA grade D erosive reflux esophagitis

    • Or patients having a clinically indicated pH/impedance monitoring on proton pump inhibitor therapy for indications of gastroesophageal reflux disease.

    Exclusion criteria:
    • Neoplasm of the esophagus or stomach

    • Use of drugs that interfere with CYP2C19 metabolism Diazepam, phenytoin, amitriptyline, clomipramine, clopidogrel Cyclophosphamide, progesterone, fluoxetine, fluvoxamine, ketoconazole Lansoprazole, omeprazole, ticlopidine

    • Evidence of active H. pylori infection

    • Inability to read due to: Blindness, cognitive dysfunction, or English language illiteracy

    • Disorders which predispose to unreliable responses such as Schizophrenia, Alzheimer's disease or significant memory loss

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Mayo Clinic in Rochester Rochester Minnesota United States 55905

    Sponsors and Collaborators

    • Mayo Clinic

    Investigators

    • Principal Investigator: David Katzka, MD, Mayo Clinic

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    David A. Katzka, Principal Investigator, Mayo Clinic
    ClinicalTrials.gov Identifier:
    NCT01824199
    Other Study ID Numbers:
    • 12-008053
    First Posted:
    Apr 4, 2013
    Last Update Posted:
    Oct 11, 2017
    Last Verified:
    Oct 1, 2017
    Keywords provided by David A. Katzka, Principal Investigator, Mayo Clinic
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 11, 2017