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CHORUS - Comprehensive HHT Outcomes Registry of the United States (Formerly OUR HHT Registry)
Sponsor: Unity Health Toronto
Summary
The goal of this study is to better understand HHT, the symptoms and complications it causes ("outcomes") and how the disease impacts people's lives. The investigators are aiming to recruit and gather information together in the Registry from 1,000 HHT patients from four HHT Centres of Excellence in North America. The Investigators will collect long-term information about the people in the Registry, allowing the investigators to understand how the disease changes over time, and what factors can influence those changes. Ultimately, this should help improve treatments for the disease.
Official title: Hereditary Hemorrhagic Telangiectasia (HHT) Research Outcomes Registry
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
296
Start Date
2018-11-01
Completion Date
2028-06-30
Last Updated
2025-04-16
Healthy Volunteers
No
Interventions
Registry and Saliva sample
Non-interventional registry with saliva sample collected for DNA analysis
Locations (1)
St. Michael's Hospital
Toronto, Ontario, Canada