Evaluation of Hemostasis in Bleeding and Thrombotic Disorders
Start Date
10/1/2002
Completion Date
1/1/2028
Summary
The objective of this study will be to assess the coagulation system in-vitro in a variety of bleeding and clotting disorders using the ROTEG analyzer and the thrombin generation assay.
Detailed Description
This is an exploratory study involving blood coagulation assays in a select group of individuals receiving treatment for their congenital or acquired bleeding or clotting disorder at UTHealth Houston. The ROTEG is a newly developed coagulation analyzer which allows the continuous assessment of whole blood coagulation from the formation of the first fibrin fibers and activated platelets, to the formation of a three-dimensional whole blood clot until the eventual dissolution of the clot. This device will not be used as a diagnostic or procedure tool. No recommendations regarding interpretation of the results or implications for future treatment will be provided.
Eligibility Criteria
Age Range: No minimum to 98 years
Conditions
Locations
The Univerisity of Texas Health Science Center at Houston
Houston, Texas 77030
United States
UT Physicians Women's Center-Texas Medical Center
Houston, Texas 77030
United States