recurrent miscarriage
Conditions
Interventions
None listed
Sponsors
Academisch Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: participation in the previously performed ALIFE study (Kaandorp, NEJM, 2010)
Exclusion criteria
Exclusion criteria: none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primairy study parameters are: - Annexin A5 M2 haplotype and live birth in these women in different treatment arms in the ALIFE trial - Anti β2 glycoprotein antibodies and live birth in these women in different treatment arms in the ALIFE trial - HCGβ and LHβ gene variants and live birth in these women | — |
Secondary
| Measure | Time frame |
|---|---|
| Secundary study parameters are: - Annexin A5 M1 haplotype Biobank containing DNA, RNA, citrated blood, heparin blood, EDTA blood, serum and plasma of women with recurrent miscarriage | — |
Countries
Netherlands
Outcome results
None listed