Last updated on March 2019

Registry of Outcomes From AntiReflux Surgery

Brief description of study

Prospective registry comparing outcomes after laparoscopic treatment of gastroesophageal reflux disease and hiatal hernia.

Detailed Study Description

This is a prospective, multi center, observational database of patients that are having surgical laparoscopic antireflux procedure and/or hiatal hernia repair, including laparoscopic Nissen fundoplication and Magnetic Sphincter Augmentation with the LINX device. Patients meeting registry inclusion and exclusion will be followed for 5 years with standardized quality of life surveys and appropriate standard of care testing. Up to 40 sites will participate with total enrollment of 1000 patients.

The main objectives are to collect data from everyday clinical practices and track patients from preoperative assessments to 5 years post surgical intervention to evaluate symptoms, medication use and side effects.

Clinical Study Identifier: NCT02923362

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Mayo Clinic

Jacksonville, FL United States
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Bass Medical Group

Walnut Creek, CA United States
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Swedish Health Services

Seattle, WA United States
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Keck Hospital of USC

Los Angeles, CA United States
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Advanced Surgeons, PC

Birmingham, AL United States
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Albany Surgical PC

Albany, GA United States
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Tampa Bay Reflux Center

Riverview, FL United States
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Affinity Medical Group

Chilton, WI United States
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