Efficacy Of Hiatal Closure For GERD

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-50
SponsorUniversity of Chicago

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 volunteers

Qualifiers

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

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Concentration of pH testing

Determine GERD remission for hiatal closure alone for patients with pH proven GERD

Time frame
at 1 and 2 years

Secondary outcomes

Other outcomes

Sponsors and contacts

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