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

  • Congenital or Acquired Bleeding Disorder Congenital or Acquired Thrombotic Disorder

Exclusion Criteria

  • Poor venous access

Study Design

Phase
Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Recruiting Locations

The Univerisity of Texas Health Science Center at Houston
Houston, Texas 77030
Contact:
Katherine Addy, RN, BSN, MPH
713-500-8352
Katherine.E.Addy@uth.tmc.edu

More Details

Status
Recruiting
Sponsor
The University of Texas Health Science Center, Houston

Study Contact

Katherine Addy, RN, BSN, MPH
713-500-8352
Katherine.E.Addy@uth.tmc.edu

Detailed Description

This is an exploratory study involving blood coagulation assays in a select group of individuals. 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.