Infertility. Complication associated with artificial fertilization, unspecified
Conditions
Interventions
Intervention 1: Intervention group: Trigger with 0.2 mg deca peptil ampoule and 6500 HCG ampoule 40 and 34 hours before oocyte retriveal. Intervention 2: Intervention group: Trigger by standard method
Sponsors
Yazd University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 42 Years
Inclusion criteria
Inclusion criteria: normal responder women Age less than 42 years BMI <30 Kg / m2 Estradiol Trigger Doses between 500 and 3000 pg / ml
Exclusion criteria
Exclusion criteria: Severe male factor Untreated thyroid disorders Severe uterine anomaly Existence of pco criteria FSH> 10 days of the third menstrual cycle and AMH <1 BMI less than 18 and more than 35 Predicting the the chance of of ovarian hyper stimulation syndrom(OHSS) Hyperprolactinemia Endocrine Disorders Congenital adrenal hyperplasia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number of follicles. Timepoint: From the tenth day of the cycle. Method of measurement: sonography.;Number of recovered oocytes. Timepoint: Oocyte recovery day. Method of measurement: observation.;Number of canceled cycles. Timepoint: Oocyte recovery day. Method of measurement: observation.;Number of embryo. Timepoint: 2 days after Oocyte recovery. Method of measurement: observation.;Embryo grading. Timepoint: 3 days after Oocyte recovery. Method of measurement: observation.;Number of transfered embryo. Timepoint: embryo transfere day. Method of measurement: observation. | — |
Secondary
| Measure | Time frame |
|---|---|
| Chemical pregnancy rate. Timepoint: 14 days after embryo transfer. Method of measurement: positive B-HCG.;Clinical pregnancy rate. Timepoint: 4 weeks after embryo transfer. Method of measurement: fetal heart rate in sonography. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr maryam Mortazavi
Yazd University of Medical Sciences
Outcome results
None listed