Infertility
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Subjects for the first ICSI cycle; 2. Aged younger than 35 years; 3. BMI 18-25 kg/m2; 4. Normal ovarian response (AFC: 6-15; basal FSH =10 IU/L; E2 14 mm under ultrasound on the hCG day; 7. Normal uterine cavity under ultrasound; 8. Subject must have read and signed the Informed Consent form.
Exclusion criteria
Exclusion criteria: 1. Husband/partner of the subject with oligospermia and asthenospermia due to genetic disorders; 2. Subject or her husband/partner with chromosomal abnormalities; 3. Subjects with abnormal, undiagnosed gynecological bleeding or with genitourinary malformations; 4. Subjects with clinically significant systemic disease; 5. Subjects with any contraindication to COS for ART or to gonadotropins; 6. Planned freeze all cycle (oocytes or embryos); 7. Subjects with hydrosalpinx (uni- or bilateral), endometriosis (grade III–IV) or recurrent miscarriage; 8. Concurrent participation in another clinical study; 9. Less than four 2PN zygotes obtained after ICSI.
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| The number of embryos utilized;The number of good quality embryos;The number of non-viable embryos;Clinical pregnancy;Biochemical pregnanacy;Ongoing pregnancy;Multiple pregnancy;Ectopic pregnancy;Spontaneous miscarriage; | — |
Primary
| Measure | Time frame |
|---|---|
| Implantation; | — |
Countries
China
Contacts
Chongqing Health Center for Women and Children