The Johns Hopkins Heartburn Center Registry

Status

Enrolling by invitation

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03853772

Enrollment

2000

Registered

2019-02-26

Start date

2019-04-27

Completion date

2028-12-01

Last updated

2026-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Barrett Esophagus, Esophagitis, Gastroesophageal Reflux Disease, Laryngopharyngeal Reflux

Brief summary

A multi-center, multi-year registry of patients with gastroesophageal reflux disease (GERD) undergoing diagnostic evaluation and/or treatment of GERD and associated diseases and complications.

Detailed description

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.

Interventions

None listed

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame	Description
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.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORMarcia Canto, MD

Johns Hopkins University

Outcome results