Phase
Condition
Anemia
Lupus
Venous Thromboembolism
Treatment
treatment "standard"
treatment "intervention"
biological assessment
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Patient aged ≥ 18 years
Patient with a diagnosis of primary or secondary autoimmune hemolytic anemia (AIHA) (infections, hematologic diseases, systemic diseases), according to the followingcriteria:
Hemoglobin <12 g/dL
and decreased haptoglobin (<0.4 g/L)
and positive direct antiglobulin test (direct Coombs test) (IgG +/- C3d)
Patient newly diagnosed or relapse
Patient with an estimated life expectancy of more than 6 months
Patient who provided free, written and informed consent
Exclusion
Exclusion Criteria:
Patients with immediate symptomatic VTE, confirmed by appropriate complementaryexaminations (venous Doppler of the lower limbs, thoracic angioscanner or pulmonaryscintigraphy).
Patients on curative anticoagulation (venous thromboembolic disease, atrialfibrillation)
Patient on dual antiaggregation treatment
Patient with active bleeding
Patient with a known condition or lesion at risk of bleeding
Patient with ischemic stroke with hemorrhagic transformation within 6 months priorto inclusion
Patient on preventive anticoagulation for 14 days or more
Patient with a contraindication to apixaban:
Known hypersensitivity to the molecule or to any of the excipients,,
thrombocytopenia <100 G/L,
kidney failure (glomerular filtration rate < 30 ml/min/1.73m²)
Active liver disease (liver failure defined as Factor V <50% or INR >1.5, ALTelevation >2 times the upper limit of normal)
Patients receiving concomitant CYP3A4 inducers (rifampin, phenytoin, carbamazepine,phenobarbital, St. John's Wort) or CYP3A4 inhibitors (azole antifungals, HIVprotease inhibitors), if these therapies cannot be discontinued or modified
Patients with a contraindication to enoxaparin:
allergy to the drug
history of heparin-induced thrombocytopenia
Patient with cold agglutinin-related AHAI (C3d-positive ADT alone withidentification of cold agglutinins)
Patient with severe disorders of hemostasis:
hypofibrinogenemia < 2 g/L,
disseminated intravascular coagulation (APTT prolongation>1.2, and PT<50%, andthrombocytopenia<100 G/L, and D-Dimer >500 µg/L)
hemophilia
Patient whose clinical condition requires hospitalization in an intensive care unit
Patient who has already participated in the study
Patient not affiliated to national health insurance
Patient under legal protection (curatorship, guardianship)
Patient subject to a measure of legal protection
Pregnant, parturient or breastfeeding women
Patient with physiological capacity to procreate (having had her first menstrualperiod and not menopausal and not presenting permanent sterility (hysterectomy,bilateral salpingectomy, bilateral oophorectomy)) and unable to have effectivecontraception (i.e., provided by an estrogen-progestin oral contraceptive orprogestogen, a contraceptive implant, an intrauterine device or a tubal ligation)
Patient of legal age who is unable to provide consent
Study Design
Connect with a study center
Chu Dijon Bourgogne
Dijon, 21000
FranceActive - Recruiting
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