Southeastern ATTR Amyloidosis Consortium: SEATTRAC Family Registry
Starting soon
Conditions studied: Amyloidosis, Hereditary
In brief
The study design is a prospective registry including asymptomatic and symptomatic patients who carry a pathogenic TTR mutation. The study will enroll patients who meet the inclusion criteria and none of the exclusion criteria until 1000 patients are enrolled, at which point in time the study investigators will evaluate whether further patient accrual is meaningful.
Key facts
- Study ID
- NCT05974644
- Run by
- Virginia Commonwealth University
- People needed
- 1000
- Starts
- 2026-07-01
- Expected to finish
- 2030-12-01
- Last updated by the study team
- 2026-06-09
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Over the age of 18 years
- Carrier of a pathogenic hATTR mutation confirmed on whole blood gene testing or mass spectrometry
- Willing to return for required follow-up visits
You may not qualify if…
- Patient having undergone heart transplantation or implantation of mechanical circulatory support
- Patients unable to provide informed consent
- Patients having undergone liver transplantation
- Patients have evidence of light chain amyloidosis
Where it is running
- Virginia Commonwealth University — Richmond, Virginia, United States
Full record on ClinicalTrials.gov
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