CYP2C19 Genotype Predictor of Gastric Acid Suppression

EARLY_PHASE1WithdrawnINTERVENTIONAL
0
Timeline

Start Date

March 31, 2013

Primary Completion Date

November 30, 2016

Study Completion Date

November 30, 2016

Conditions
Esophagitis
Interventions
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.

Trial Locations (1)

55905

Mayo Clinic in Rochester, Rochester

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Mayo Clinic

OTHER

NCT01824199 - CYP2C19 Genotype Predictor of Gastric Acid Suppression | Biotech Hunter | Biotech Hunter