The Johns Hopkins Heartburn Center Registry
Trial Snapshot
- Phase
- Not Applicable
- Status
- Enrolling By Invitation
- Sponsor
- Enrollment
- 2,000
- Locations
- 9
- Primary Endpoint
- Demographic and clinical data obtained via chart review and questionnaires
Study Overview
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.
Study Design
- Study Type
- Observational
- Observational Model
- Case Only
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
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
Outcomes
Primary Outcomes
Demographic and clinical data obtained via chart review and questionnaires
Time Frame: 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.
Secondary Outcomes
No secondary outcomes reported