Back to search results
NCT03853772

The Johns Hopkins Heartburn Center Registry

Enrolling by Invitation
Not specifiedAges 18+Observational
Johns Hopkins University
~2,000 participants
Updated 2026-08-26 on ClinicalTrials.gov

At a glance

Recruiting sites
0 of 9 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Demographic and clinical data obtained via chart review and questionnaires
Measured over 5 years

Conditions

Gastroesophageal Reflux Disease
Barrett Esophagus
Laryngopharyngeal Reflux
Esophagitis

Explore related trials

Barrett EsophagusEsophagitisGastroesophageal Reflux DiseaseLaryngopharyngeal reflux

NCT03853772

Where you'd take part

This study runs at 9 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Fox Valley Surgical Associates

    Appleton, Wisconsinno site contact published

  • Geisinger

    Danville, Pennsylvaniano site contact published

  • Johns Hopkins Hospital

    Baltimore, Marylandno site contact published

  • Mayo Clinic

    Rochester, Minnesotano site contact published

  • The Matagorda Regional Medical Group

    Bay City, Texasno site contact published

  • UCI-Irvine

    Orange, Californiano site contact published

  • UNRMed-University of Nevada, Reno

    Reno, Nevadano site contact published

  • UT Health

    Houston, Texasno site contact published

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Study leadership

  • Marcia Canto, MD · PRINCIPAL_INVESTIGATOR · Johns Hopkins University

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

Want this trial checked against your situation?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

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

Exclusion

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

What this trial measures

  • Demographic and clinical data obtained via chart review and questionnaires5 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.