Infertility treated by ICSI Pregnancy and Childbirth In vitro fertilization
Conditions
Interventions
The number of patients included in both groups was chosen based upon a special statistical calculation which makes the outcome of the study meaningful. After the pre-calculated number is reached the s
Sponsors
The Egyptian IVF Center (Egypt)
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Women under 40 years old undergoing intracytoplasmic sperm injection (ICSI) in the first or second trial and using the long GnRHa protocol
Exclusion criteria
Exclusion criteria: 1. Donor eggs 2. Patients aged 40 or older 3. Pre-implantation Genetic Diagnosis (PGD) cycles 4. Patients with fibroids or congenital anomalies of the uterus
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical pregnancy rate, which is measured by BhCG assay 2 weeks after embryo transfer followed by ultrasound at 6?7 weeks to detect fetal echoes and pulsation | — |
Secondary
| Measure | Time frame |
|---|---|
| Ongoing pregnancy rate, which is diagnosed by ultrasound examination at 20?24 weeks pregnancy to document a viable pregnancy at this point | — |
Countries
Egypt
Outcome results
None listed