Clinical Trials Directory

Trials / Completed

CompletedNCT00315471

Determining Disease Activity Biomarkers in Individuals With Takayasu's Arteritis

VCRC Longitudinal Protocol for Takayasu's Arteritis

Status
Completed
Phase
Study type
Observational
Enrollment
224 (actual)
Sponsor
University of Pennsylvania · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Takayasu's arteritis is a rare disorder that causes swelling and damage to the large arteries in the body, such as the aorta. In order to ensure proper treatment, measuring disease activity is critical. The purpose of this study is to establish new biological markers (biomarkers) to assess the severity of disease in people with Takayasu's arteritis.

Detailed description

Takayasu's arteritis is a chronic inflammatory condition that affects the aorta, the largest blood vessel in the body, and its branches. Inflammation causes segments of the vessels to become narrowed, blocked, or even stretched, possibly resulting in aneurysms. The disease is very rare but most commonly occurs in young Asian women. Symptoms may include arm pain with use, decreased or absent pulses, lightheadedness or dizziness, headaches, and visual disturbances. Many individuals with Takayasu' arteritis, however, have no apparent symptoms despite disease activity. Additionally, current tests used to measure vessel inflammation are considered unreliable and inconsistent. It is therefore very difficult to determine the extent of disease activity in a person with Takayasu's arteritis. This study will use novel scientific methods to establish new biomarkers that can be used to monitor disease activity in individuals with Takayasu's arteritis. These biomarkers may be used to help direct clinical care and assist in future drug development. Study visits will occur monthly for the first year, then every 3 months thereafter for the remainder of the study. Blood and urine collection will occur at every visit. A physical examination, disease assessment, and review of medications will occur every 3 months; participants may also be asked to complete various questionnaires. Diagnostic testing, which may include chest radiograph, echocardiogram, magnetic resonance imaging, or angiography, will occur every 6 months. Tobacco, alcohol, and drug use will be assessed on a yearly basis. Participants may have additional study visits if a disease flare or disease-related complications occur during the study.

Conditions

Timeline

Start date
2006-04-01
Primary completion
2019-12-01
Completion
2019-12-01
First posted
2006-04-18
Last updated
2022-07-12

Locations

9 sites across 2 countries: United States, Canada

Source: ClinicalTrials.gov record NCT00315471. Inclusion in this directory is not an endorsement.