The Johns Hopkins Heartburn Center Registry

This registry is a prospective, multicenter registry of patients undergoing diagnostic evaluation and/or treatment of gastroesophageal reflux disease and associated diseases and complications.

Patients who are eligible will have disease and therapy-specific data collected throughout treatment and long-term (5-year) follow-up.

Electronic data capture via REDCap will be utilized for all sites.

Primary outcomes

• Demographic and clinical data obtained via chart review and questionnaires [5 years]: Establish a registry with collected data related to patients undergoing diagnostic evaluation and treatment of GERD and its associated diseases in multiple academic and community settings.

Sex: All, ages: 18 Years to any

Inclusion Criteria:

* Referred GERD patients willing to participate in long term follow-up (5 years)

Exclusion Criteria:

* Potential participants will be excluded if unwilling or unable to complete surveillance questionnaires through this registry

• Marcia Canto, MD, Principal investigator, Johns Hopkins University