Assisted Reproductive Technology, Infertility, IVF
Conditions
Brief summary
Prospective, open, randomized, parallel, two-arm trial to compare the clinical pregnancy rate between most commonly used two embryo transfer techniques: trial followed by transfer technique and afterloading technique
Detailed description
Eligible patients will be informed about the possibility of participating in the clinical trial in the beginning of treatment and on the day ET, a signed consent form will be collected from those recipients who confirmed their participation. These patients will be randomized immediately before the ET procedure by sequentially numbered, opaque, sealed envelopes
Interventions
Embryo transfer is done by using afterload transfer method
Embryo transfer is done by using afterload transfer method
Sponsors
Study design
Intervention model description
Prospective, open, randomized, parallel, two-arm trial
Eligibility
Inclusion criteria
1. Patient has given written informed consent 2. BMI 18-30 kg/m2 3. \< 2 previous failed IVF trials 4. At least two good quality embryos on the day of transfer
Exclusion criteria
1. Congenital uterine anomaly 2. Untreated endometrial polyp or fibroid distorting uterine cavity 3. Presence of hydrosalpinx 4.2 or more prior IVF trial failure 5.Moderate to severe endometriosis 6.Recurrent pregnancy loss history
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| clinical pregnancy rate | 5-6 weeks after embryo transfer | the presence of gestational sac on ultrasound |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| implantation rate | 3-4 weeks after embryo transfer | the number of gestational sacs divided by the number of embryos transferred |
Countries
Turkey (Türkiye)