Infertility, Female
Conditions
Keywords
suboptimal response, Corifollitropin alfa, IVF, Ovarian stimulation
Brief summary
In an opened randomized study of women undergoing in vitro fertilization with expected suboptimal response to controlled ovarian stimulation (Poseidon Group 2b) investigators will examine clinical efficacy and safety of two stimulation protocols: Corifollitropin alfa (Elonva) in combination with menotropin (Merional) versus Follitropin alfa and lutropin alfa (Pergoveris).
Detailed description
Patients, found eligible for the study, will be randomized (envelope method) into two arms in 1:1 ratio at the start of stimulation (menstrual cycle day 2-3, randomization day): Arm A - ovarian stimulation with Corifollitropin alfa in combination with menotropin; Arm B - ovarian stimulation with Follitropin alfa and lutropin alfa. At the first day of controlled ovarian stimulation (COS) participants in the first group will receive a single injection of Corifollitropin alfa 150 mcg followed by daily menotropin administration at the dose of 150 international unit (IU) from stimulation day 1 to day 7 and at the dose of 300 IU from day 8 up to the end of stimulation. Ovarian stimulation in group B will be performed with daily 300 IU of Follitropin alfa and lutropin alfa starting on menstrual cycle day 2-3. For all subjects, a fixed dose of gonadotropin-releasing hormone (GnRH) antagonist will be injected daily as soon as one of the follicles reaches the ≥14 mm diameter and stopped one day before oocyte pick up (OPU); ovulatory dose of human chorionic gonadotropin (hCG) could be administered when at least one follicle reaches 16.5 mm in diameter. Retrieved oocytes following fertilization (conventional IVF or ICSI) will be cultured to morula or blastocyst stage followed by ultrasound guided single or double embryo transfer (ET day, performed 4-5 days after OPU).
Interventions
DRUGCorifollitropin alfa and menotropin
Procedure: Ovarian stimulation is performed by the combination of a single Corifollitropin alfa 150 mcg injection on menstrual cycle day 2-3 and daily menotropin administration at the dose of 150 IU from stimulation day 1-7 and at the dose of 300 IU from day 8 to the end of stimulation (maximal dose adjustment to 450 IU). Other interventions: conventional GnRH antagonist protocol and in vitro fertilization (IVF/ICSI) cycle
Procedure: Ovarian stimulation is performed with daily 300 IU of Follitropin alfa and lutropin alfa starting on menstrual cycle day 2-3. Maximal allowed dose adjustment is 450 IU daily. Other interventions: conventional GnRH antagonist protocol and in vitro fertilization (IVF/ICSI) cycle.
Sponsors
D.O. Ott Research Institute of Obstetrics, Gynecology, and Reproductology
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
35 Years to 41 Years
Healthy volunteers
No
Inclusion criteria
* Female age between 35-41 years; * BMI 17,5-30 kg/m2; * Expected suboptimal responders (according to Poseidon classification, 2016, Group 2b): patients with suboptimal ovarian reserve prestimulation parameters in terms of antimüllerian hormone (AMH) and antral follicle count (AFC): AFC 5-9, AMH ≥0.8 ng/mL; * Early follicular phase follicle stimulating hormone (FSH) ≤15 IU/L; * Presence of viable spermatozoa in partner's sperm; * Signed informed consent.
Exclusion criteria
* Pre-existing medical condition preventing or interfering with IVF treatment: any clinically significant systemic disease; inherited or acquires thrombophilia and thromboembolism; endocrine or metabolic abnormalities; moderate or severe impairment of renal or hepatic function; any oncological diseases in anamnesis; known history of recurrent miscarriage, abnormal karyotype of both partners; currently active pelvic inflammatory disease; * Abnormal IVF screening tests: Papanicolaou test, Syphilis, HIV 1&2, Hepatitis B, Hepatitis C, Chlamydia, and Gonorrhea; * Presence of uterine pathology: Asherman's Syndrome, endometrial polyps, nodus form of adenomyosis or uterine fibroids ≥3 mm in diameter; * Visualization of ovarian cysts ≥25 mm, endometriomas or hydrosalpinx; * One or more follicles ≥8 mm on randomization day.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of cumulus-oocyte complexes (COCs) | 3-4 weeks after ET | Number of COCs, obtained during oocyte pick up (OPU), after controlled ovarian stimulation (COS) in two protocols |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of participants with optimal or suboptimal response to COS | 2-4 weeks after randomization | ≥ 5 COCs at at oocyte recovery day |
| Cycle cancellation rate | 6-7 weeks after randomization | number of cancelled cycles during COS (no response), at OPU (premature ovulation, absence or degradation of COCs), during in vitro cultivation (fertilization failure, inadequate embryo quality) or due to other reasons (adverse events, ovarian hyperstimulation syndrome (OHSS), withdrawal) |
| Frequency of side reactions | 2-4 weeks after randomization | number of patients with local reactions (redness, itching, swelling or pain) or abdominal discomfort evaluated using visual analogue scale at the end of COS and at ET day |
| Implantation rate | 3-4 weeks after ET | ratio of the number of intrauterine gestational sacs to the number of transferred embryos |
| Clinical pregnancy rate | 5-6 weeks after randomization | presence of intrauterine gestational sac at transvaginal ultrasound measured per embryo transfer |
| Duration of stimulation | 2-4 weeks after randomization | total days of COS: from the first gonadotropins administration to ovulation triggering |
| Number of follicles at the end of stimulation | 2-4 weeks after randomization | measured for follicles ≥17 mm and ≥14 mm |
| Dose adjustment frequency | 2-4 weeks after randomization | number of participants with menopausal or recombinant human follicle stimulating hormone (FSH) dose increase |
| Number of mature (MII) oocytes | 2-4 weeks after randomization | assessment is done only for ICSI cycles at oocyte recovery day |
Other
| Measure | Time frame | Description |
|---|---|---|
| Embryo quality | 3-5 days after oocyte recovery | number of best and good quality embryos per transfer |
| Cost-effectiveness of COS | 6-7 weeks after randomization | ratio of total cost of stimulation (on investigated drugs) to the number of patients with clinical pregnancy |
| Fertilization rate | 1 day after OPU | number of two-pronuclear zygotes on day 1 after fertilization |
| Biochemical pregnancy rate | 3-4 weeks after ET | positive ß-hCG test (≥30 IU/L) following ET without clinical pregnancy confirmation |
Countries
Russia
Outcome results
None listed