infertility. Female infertility, unspecified
Conditions
Interventions
Intervention 1: Control group: Patients who candidate for microinjection (ICSI), underwent for induction of ovulation, underwent by long protocol in the beginning of cycle. Determination of uterus dep
Colorado, USA) was used for all embryo culturing. Embryo scoring was done according to zonal thickness, cytoplasm fragmentation, blastomeres number, and morphology. The clinician also made sure that t
Treatment - Drugs
Control group: Patients who candidate for microinjection (ICSI), underwent for induction of ovulation, underwent by long protocol in the beginning of cycle. Determination of uterus depth was done for
Intervention Group also followed the same procedure as control groups and the same medications were used. In addition, 20 mg daily prednisolone was given to all Intervention Group, One day before the
Sponsors
Urmia University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: i nclusion criteria: having infertility;FSH serum levels lower than 10 ,age of lower than 42 years exclusion criteria: having asthma; systemic disorders; gastrointestinal disorders
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Abortion. Timepoint: until 20 weeks. Method of measurement: observation.;Intra uterus pregnancy. Timepoint: 12,20 weeks. Method of measurement: sonography.;Chemical pregnancy. Timepoint: 6 weeks. Method of measurement: BHCG mesuring. | — |
Secondary
| Measure | Time frame |
|---|---|
| None. Timepoint: none. Method of measurement: none. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFariba Nanbakhsh
Reproductive Health Research Center
Outcome results
None listed