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ACTIVE NOT RECRUITING
NCT04150822

CHORUS - Comprehensive HHT Outcomes Registry of the United States (Formerly OUR HHT Registry)

Sponsor: Unity Health Toronto

View on ClinicalTrials.gov

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

OTHER

Registry and Saliva sample

Non-interventional registry with saliva sample collected for DNA analysis

Locations (1)

St. Michael's Hospital

Toronto, Ontario, Canada