About this trial
The purpose of this protocol is to study the efficacy of hiatal closure for early GERD disease. The study team hypothesizes that hiatal closure for early GERD disease is an efficacious treatment of GERD.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age 18 - 50 years
Able to provide informed consent
BMI <30
Hiatal defect <4cm on esophagram
Disqualifiers
Vulnerable subjects (children, prisoners, pregnant women) will be excluded.
Trial population
The estimated annual number of subjects enrolled prospectively in the study is 20. The recruitment goal is 40. The research team will screen all patients that are being followed-up at the gastrointestinal surgery clinic at the UCM.
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Concentration of pH testing
Determine GERD remission for hiatal closure alone for patients with pH proven GERD
Sponsors and contacts
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