Effect of HCQ on AnxA5 Resistance Assay in Antiphospholipid (aPL) Positive Patients With and Without Systemic Lupus Erythematosus (SLE)
NCT ID: NCT01475149
Last Updated: 2017-03-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
33 participants
OBSERVATIONAL
2010-09-30
2016-08-31
Brief Summary
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Detailed Description
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This 12 week study will observe patients with persistent aPL in the blood who are starting a medicine called hydroxychloroquine (HCQ). The primary goal of the study is to compare results of the AnxA5 resistance assay from patients before they start taking HCQ and after they have taken it for 12 weeks to see if the results of the blood test change. Our secondary goal is to measure a variety of other blood tests before and after patients have started taking HCQ; these tests include D-dimer, Activated Protein C (APC) Resistance, and aPL titers/status (LA test, aCL ELISA, aß2GPI ELISA, and anti-Domain-I ß2GPI ELISA).
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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aPL positive - group 1
aPL positive with APS, receiving HCQ
Phlebotomy
Subjects will have blood drawn at each of the 3 study visits.
aPL positive - group 2
aPL positive with APS and SLE, receiving HCQ
Phlebotomy
Subjects will have blood drawn at each of the 3 study visits.
aPL positive - group 3
aPL positive without APS but with SLE, receiving HCQ
Phlebotomy
Subjects will have blood drawn at each of the 3 study visits.
aPL positive - group 4
aPL positive without APS or SLE, receiving HCQ
Phlebotomy
Subjects will have blood drawn at each of the 3 study visits.
aPL negative - group 1
aPL negative with SLE, receiving HCQ
Phlebotomy
Subjects will have blood drawn at each of the 3 study visits.
aPL negative - group 2
aPL negative with SLE, not receiving HCQ
Phlebotomy
Subjects will have blood drawn at each of the 3 study visits.
Interventions
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Phlebotomy
Subjects will have blood drawn at each of the 3 study visits.
Eligibility Criteria
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Inclusion Criteria
* new HCQ (200-400 mg/day) treatment (for all but 5 of 10 control subjects - see below)
* persistently positive aPL
Exclusion Criteria
* Heparin use at the time of enrollment
* Any immunosuppressive drug use within 3 months prior to screening
* HCQ use within the past 6 months prior to screening visit
* Another antimalarial agent treatment,
* Pregnant women, minors, mentally disabled, prisoners
* Acute thrombosis within 2 weeks prior to screening
18 Years
65 Years
ALL
No
Sponsors
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Montefiore Medical Center
OTHER
Hospital for Special Surgery, New York
OTHER
Responsible Party
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Principal Investigators
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Doruk Erkan, MD
Role: PRINCIPAL_INVESTIGATOR
Hospital for Special Surgery, New York
Locations
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Hospital for Special Surgery
New York, New York, United States
Countries
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Other Identifiers
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IRB 10130
Identifier Type: -
Identifier Source: org_study_id
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