156 Million Patient Visits, Endless Research Possibilities
Reg-ent’s dataset spans more than 156 million patient visits, representing care delivered directly by Reg-ent participants, and includes over 16.7 million patients overall. This makes it the most comprehensive otolaryngology-specific data repository in the country. Participants can leverage this data for peer-reviewed research and quality improvement initiatives.
Contribute to Specialty-Advancing Research
Participating members and their practices across the United States have shared structured and unstructured EHR data as well as ancillary data (audiograms, Patient Reported Outcomes (PROs), radiology reports, and laboratory reports).
Collecting and maintaining this data set maintains our ability to study and define optimal clinical quality for the specialty, which will be critical for continued reimbursement advocacy efforts. The comprehensiveness of the data repository also allows for robust, up to date data for research purposes.
Unique Patients
Patient Visits
Clinicians
Years of Data
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For Participants
Learn how to submit research proposals or request data and review the submission requirements and policies.
For Industry Partners
Access specialty-specific ENT datasets and unique use cases that only Reg-ent can provide.
Partner opportunities coming soon.
Publications
Explore how Reg-ent data is advancing research. Browse published studies, review current projects, and discover insights.