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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00616317
Other study ID # 235519
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 2006
Est. completion date January 2040

Study information

Verified date June 2023
Source University of California, Davis
Contact Lavjay Butani
Phone (916) 734-8118
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to gather information about causes and treatment of Antiphospholipid Syndrome.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date January 2040
Est. primary completion date January 2040
Accepts healthy volunteers No
Gender All
Age group 1 Minute to 18 Years
Eligibility Inclusion Criteria: - 18 years of age or younger at the onset of disease - Presence of Vascular Thrombosis - UC Davis patient - Presence of at least one Laboratory criteria including: Anticardiolipin antibody, Anti-B glycoprotein-I antibody or Lupus anticoagulant in plasma Exclusion Criteria: - Infants born to mothers with APS - Infants with congenital thrombophilia

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States UC Davis Medical Center Sacramento California

Sponsors (2)

Lead Sponsor Collaborator
University of California, Davis Ministry of Higher Education, Science and Technology, Solvenia

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Long term survival 10 year
See also
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