Abortion. Supervision of pregnancy with history of abortive outcome
Conditions
Interventions
Intervention 1: Aspirin (80 mg) was administered daily to the control group. Intervention 2: the study group 5 g IVIG was initiated within 2 weeks prior to attempted conception. After conception occur
Treatment - Drugs
Aspirin (80 mg) was administered daily to the control group
the study group 5 g IVIG was initiated within 2 weeks prior to attempted conception. After conception occurred, IVIG was given every 4 weeks for up to 32 weeks of gestation. IVIG was administered in h
Sponsors
Vice chancellor of research in Mashhad University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: inclusion criteria: women with at least two abortions that had taken place naturally or with assisted reproductive techniques (ART) and who had at least one positive immunologic test for anti-cardiolipin; anti-phospholipid antibodies;anti-thyroid antibody; anti-nuclear antibody;Anti-sperm antibody. Exclusion criteria: anatomical problems; infections; hormonal factors contributing to recurrent abortion and parental factors were excluded.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Neonate. Timepoint: 9 month. Method of measurement: Delivery. | — |
Secondary
| Measure | Time frame |
|---|---|
| Abortion. Timepoint: Each time after intervention. Method of measurement: exposing symptoms of abortion.;Premature birth. Timepoint: Each time after intervention. Method of measurement: exposing symptoms of premature birth. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactmajid jafari
Mashhad University of Medical Sciences
Outcome results
None listed