Evaluation of Hemostasis in Bleeding and Thrombotic Disorders
Purpose
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.
Conditions
- Blood Coagulation Disorders, Inherited
- Thrombotic Disorder
Eligibility
- Eligible Ages
- Between 1 Day and 98 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
patients with congenital or acquired bleeding or clotting disorders who have provided informed consent and/or assent
Exclusion Criteria
poor venous access
Study Design
- Phase
- Study Type
- Observational
- Observational Model
- Other
- Time Perspective
- Prospective
Recruiting Locations
Houston, Texas 77030
Houston, Texas 77030
More Details
- Status
- Recruiting
- Sponsor
- The University of Texas Health Science Center, Houston
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.