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Register for Pediatric Patients With Antiphospholipid Syndrome (APS): European Project Extended Internationally Study (APS)

This study is currently recruiting participants.
Verified October 2016 by University of California, Davis
Sponsor:
ClinicalTrials.gov Identifier:
NCT00616317
First Posted: February 15, 2008
Last Update Posted: May 30, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Collaborator:
Ministry of Higher Education, Science and Technology, Solvenia
Information provided by (Responsible Party):
University of California, Davis
  Purpose
The purpose of this study is to gather information about causes and treatment of Antiphospholipid Syndrome.

Condition
Antiphospholipid Syndrome

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Register for Pediatric Patients With Antiphospholipid Syndrome (APS): European Project Extended Internationally Study

Resource links provided by NLM:


Further study details as provided by University of California, Davis:

Primary Outcome Measures:
  • Long term survival [ Time Frame: 10 year ]

Estimated Enrollment: 50
Study Start Date: September 2006
Estimated Study Completion Date: January 2020
Estimated Primary Completion Date: January 2020 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   up to 18 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Pediatric Nephrology Clinic at University of California, Davis
Criteria

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
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00616317


Contacts
Contact: Lavjay Butani (916) 734-8118

Locations
United States, California
UC Davis Medical Center Recruiting
Sacramento, California, United States, 95817
Sponsors and Collaborators
University of California, Davis
Ministry of Higher Education, Science and Technology, Solvenia
Investigators
Principal Investigator: Lavjay Butani, M.D. University of California, Davis
  More Information

Responsible Party: University of California, Davis
ClinicalTrials.gov Identifier: NCT00616317     History of Changes
Other Study ID Numbers: 200614666-1
First Submitted: February 4, 2008
First Posted: February 15, 2008
Last Update Posted: May 30, 2017
Last Verified: October 2016

Keywords provided by University of California, Davis:
Antiphospholipid Syndrome

Additional relevant MeSH terms:
Syndrome
Antiphospholipid Syndrome
Disease
Pathologic Processes
Autoimmune Diseases
Immune System Diseases


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