Clinical Trials Directory

Trials / Completed

CompletedNCT02623816

Symptom Control Satisfaction With Proton Pump Inhibitor Regimen

Prospective Study Assessing Patient Satisfaction of Symptom Control With Proton Pump Inhibitor Dosing Regimen

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
64 (actual)
Sponsor
MetroHealth Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The overall aim of this study is to assess if patients with persistent gastroesophageal reflux disease (GERD) symptoms receiving sub-optimal omeprazole dosing experience improvement in GERD symptoms when prescribed an optimal dosing regimen. The optimal dosing regimen is defined as taking omeprazole 30 minutes prior to the first meal of the day.

Detailed description

GERD remains a common gastrointestinal complaint, resulting in 6% of outpatient visits. The economic burden is significant with direct costs exceeding $12 billion/year and indirect cost as high as $75 billion/year. The primary aim of this study was determine whether a brief educational intervention optimizing proton pump inhibitor (PPI) dosing would reduce GERD symptoms using the gastroesophageal reflux disease symptom assessment scale (GSAS) questionnaire. Further, secondary analysis would utilize the results of the trial and combine them with costs related to uncontrolled GERD to estimated the potential economic impact.

Conditions

Interventions

TypeNameDescription
DRUGOptimal Dosing of OmeprazoleOmeprazole 20 mg

Timeline

Start date
2014-08-01
Primary completion
2015-12-01
Completion
2015-12-01
First posted
2015-12-08
Last updated
2022-10-25
Results posted
2022-10-25

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02623816. Inclusion in this directory is not an endorsement.