NotablePrimary and study completion dates: Mar 2028 to Mar 2029v34
NotablePrimary and study completion dates: Dec 2024 to Mar 2028v33
NotablePrimary and study completion dates: Dec 2023 to Dec 2024v32
NotablePrimary and study completion dates: Dec 2022 to Dec 2023v31
NotablePrimary and study completion dates: Dec 2021 to Dec 2022v30
Show 28 earlier versionsHide 28 earlier versions
2 versionsRe-verified since Aug 3, 2020, no change to tracked fieldsv28-v29
NotablePrimary and study completion dates: Dec 2019 to Dec 2021v27
MinorPrimary completion date: Jul 2019 to Dec 2019v26
Re-verified, no change to tracked fieldsv25
NotablePrimary completion date: Jul 2018 to Jul 2019
Study completion date: Dec 2018 to Dec 2019
v24
NotablePrimary completion date: Jul 2017 to Jul 2018
Study completion date: Dec 2017 to Dec 2018
v23
Re-verified, no change to tracked fieldsv22
NotablePrimary completion date: Jul 2016 to Jul 2017
Study completion date: Jul 2016 to Dec 2017
v21
Re-verified, no change to tracked fieldsv20
NotablePrimary and study completion dates: Jul 2015 to Jul 2016v19
3 versionsRe-verified since Apr 15, 2014, no change to tracked fieldsv16-v18
Study Status, Sponsor/Collaborators, Outcome Measuresv15
2 versionsRe-verified since Aug 16, 2011, no change to tracked fieldsv13-v14
NotableLead sponsor: Office of Rare Diseases (ORD) to Duke Universityv12Show 5 more changesShow less
Primary and study completion dates: Jul 2009 to Jul 2015
Study sites: 8 to 1
Eligibility criteria shortened, about 81 words
Collaborators shortened, about 12 words
Study arms: 2 to 3
Re-verified, no change to tracked fieldsv11
MinorSite details revised at 2 of 8 sitesv10
MinorStudy sites revised (8)v9
NotablePrimary and study completion dates: Dec 2008 to Jul 2009
Study sites: 5 to 8
v8
MinorSite details revised at 1 of 5 sitesv7
MinorPrimary and study completion dates: Dec 2008v6
MinorSite details revised at 1 of 5 sitesv5
Study Status, Sponsor/Collaborators, Study Design, Arms and Interventions, Eligibilityv4
Re-verified, no change to tracked fieldsv3
NotableTrial status: Not Yet Recruiting to Recruiting
Site details revised at 5 of 5 sites
v2
Study First Submitted
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Antiphospholipid antibody syndrome (APS) is characterized by the presence of antiphospholipid antibodies, which are proteins in the blood that interfere with the body's ability to perform normal blood clotting. Clinical problems associated with antiphospholipid antibodies include an increased risk for the formation of blood clots in the lungs or deep veins of the legs, stroke, heart attack, and recurrent miscarriages. It is possible that some people with APS have a genetic predisposition for developing the syndrome. This study will use a genetic strategy to identify potential inherited risk factors for the development of APS by recruiting people with APS who have family members also affected by the syndrome or by another autoimmune disorder, such as lupus or rheumatoid arthritis.