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Enrolling by invitation NCT03853772

The Johns Hopkins Heartburn Center Registry

— Observational Gastroesophageal Reflux Disease Barrett Esophagus Laryngopharyngeal Reflux Esophagitis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Gastroesophageal Reflux Disease, Barrett Esophagus, Laryngopharyngeal Reflux, Esophagitis. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

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.

Primary outcome measures

  • Demographic and clinical data obtained via chart review and questionnaires [Time frame: 5 years]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

United States · 9 centers
  • UCI-Irvine — Orange
  • Johns Hopkins Hospital — Baltimore
  • Mayo Clinic — Rochester
  • UNRMed-University of Nevada, Reno — Reno
  • Weill Cornell — New York
  • Geisinger — Danville
  • The Matagorda Regional Medical Group — Bay City
  • UT Health — Houston
  • … and 1 more center

Identifiers

NCT: NCT03853772 · IRB00201157

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗