CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 6,718 enrolled
Drug / intervention
None. Observational Study.other
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00628745
NCT00628745N/ACompleted

Transthyretin Amyloidosis Outcomes Survey (THAOS): A Global, Multi-Center, Longitudinal, Observational Survey of Patients With Documented Transthyretin Gene Mutations or Wild-Type Transthyretin Amyloidosis.

Pfizer·observational·Posted Mar 5, 2008·Updated Nov 22, 2024

In Brief

An observational study evaluating None. Observational Study. for Transthyretin Gene Mutations and Transthyretin Amyloidosis. Completed, enrolled 6,718 participants across 113 sites in 25 countries.

Detailed Summary

THAOS is a global, multi-center, longitudinal observational survey open to all patients with transthyretin amyloidosis (ATTR), including ATTR-PN (polyneuropathy), ATTR-CM (cardiomyopathy) and wild-type ATTR-CM. It is open-ended with a minimum duration of 10 years. Patients will be followed as long as they are able to participate. The principal aims of this outcome survey are to better understand and characterize the natural history of the disease by studying a large and heterogenous patient population. Survey data may be used to develop new treatment guidelines and recommendations, and to inform and educate clinicians about the management of this disease.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesArgentina, Belgium, Brazil, Bulgaria, Canada, Cyprus, Denmark, France, Germany, Israel, Italy, Japan, Malaysia, Mexico, Netherlands, Portugal, Romania, Saudi Arabia, South Korea, Spain, Sweden, Taiwan, Turkey (Türkiye), United Arab Emirates, United States
Collaborators--

Timeline

N/ACompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMar 5, 2008
Enrollment StartJan 4, 2008
Primary CompletionJun 16, 2023
Study CompletionJun 19, 2023
TodayJul 2, 2026
Enrollment to primary: 15.5 yearsPosted 18.3 years ago

Interventions

None. Observational Study.other