In vitro maturation (IVM) is an assisted reproductive technology (ART) using minimal or no ovarian stimulation. In IVM, immature oocytes at the germinal vesical (GV) or metaphase I (MI) stage retrieved from small antral follicles are cultured to reach metaphase II (MII) (ASRM, 2021). Since the first successful IVM baby was reported, subsequent studies have been mostly focused on patients with polycystic ovary syndrome (PCOS) to reduce the risks associated with ovarian stimulation such as ovarian hyperstimulation syndrome (OHSS), thromboembolic complications and ovarian torsion (Cha et al., 1991; Chian et al., 2000). Numerous IVM protocols have been applied with or without FSH or hCG priming and using one step or two steps culture system to gain the optimum oocyte maturation rate, blastulation rate and live birth rate (Sanchez et al., 2019; De Vos et al., 2021). A randomized controlled trial (RCT) conducted on women with high antral follicle count, including women with PCOS, indicated that CAPA-IVM was non-inferior to conventional IVF (Vuong et al., 2020). Studies also showed that the mental and motor development of children born after IVM was similar to that of those born after IVF and naturally conceived (Nguyen et al., 2022; Vuong et al., 2022). Additionally, IVM is considered an effective treatment for women with gonadotropin resistant ovary syndrome to have children with their own oocytes (Le et al., 2021). IVM is also a viable option for fertility preservation for women with cancer in need of urgent treatment and contraindicated to hormonal stimulation (Grynberg et al., 2022). There is little evidence on the effectiveness of IVM on women without PCOS. Junk et al have compared the effectiveness of IVM between women with polycystic ovaries (PCO) and polycystic ovary syndrome (Junk and Yeap, 2012). Women with PCO had significantly lower oocytes collected than those with PCOS (p\<0,001), maturation rate, blastocyst development rate, and clinical pregnancy rate were comparable between two groups (Junk and Yeap, 2012). Another study indicated the maturation rate after standard IVM of ovarian tissue-derived oocytes collected from cancer patients was 8-67% (Segers et al., 2020). A study conducted by Kirillova on ovarian cancer patients with normal to high ovarian reserve showed that CAPA-IVM resulted in a higher maturation rate in ovarian tissue oocytes compared to standard IVM (56% vs 36%, p=0.0045) (Kirillova et al., 2021). Recently, IVF/ICSI has been indicated in almost all infertility patients without PCOS. A randomized controlled trial on non-PCOS women with high antral follicle counts revealed no significant differences between IVM and conventional IVF regarding the ongoing pregnancy rate, live birth rate and the incidence of pregnancy and perinatal complications (Vuong et al., 2020). IVM offers numerous advantages due to the concept of using mild or no stimulation. The risk of ovarian hyperstimulation syndrome is largely eliminated, the cost of treatment is notably reduced. IVM is also more convenient as it requires fewer patient visits, ultrasounds and blood tests (Ho and Vuong, 2023). Therefore, this pilot study is to evaluate the effectiveness and safety of CAPA-IVM in ovulatory infertile women and evaluate its success rate in relation to their ovarian reserve.
1. Screening for eligibility and randomization * This trial will be conducted at My Duc Hospital, Ho Chi Minh City, Viet Nam. * Eligibility screening will be performed on the first visit. * Patients meeting the inclusion criteria will be invited to participate in the study. Patients will be provided with study information and consent forms. The investigator will collect signed consent forms from all participants. 2. Oocyte retrieval: On days 2-4 of the menstrual cycle, after patients have consented to CAPA-IVM, they will undergo oocyte aspiration anytime thereafter but no later than day 6 of the cycle. Cycle programming with oral contraceptives or progestogens, nor ovarian stimulation with rFSH or hMG preparations nor the use GnRH analogues are allowed. The use of oral contraceptives will be considered from the second cohort of patients onwards in case the timing/scheduling of the oocyte retrieval needs to be optimized. No hCG or GnRH agonist preparations will be administered for triggering ovarian maturation prior to oocyte retrieval. 3. Capacitation in vitro maturation The follicular aspirates are collected and filtered through a cell strainer. After collection, COCs are washed and transferred to a four-well dish, containing CAPA medium. Following 24 hours of incubation in CAPA media, COCs complexes are cultured in IVM medium for 30 hours. Following IVM culture, oocytes are mechanically and enzymatically denuded from their cumulus layers under a stereomicroscope and oocyte maturation is assessed under the inverted microscope 4. Fertilization: ICSI will be used to fertilize mature oocytes. Embryos will be cryopreserved at the cleavage-stage embryo (day 3) if the patient has less than 4 embryos. Patients with 4 or more embryos will be counseled on blastocyst culture (day 5) according to the IVFMD protocol. All viable embryos will be cryopreserved.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
On days 2-4 of the menstrual cycle, after patients have consented to CAPA-IVM, they will undergo oocyte aspiration anytime thereafter but no later than day 6 of the cycle. Pre-maturation will last for 24-30 hours. ICSI will be used for insemination. Freeze-only on day 3 or day 5 and frozen embryo transfer will be performed on the subsequent cycle using HRT protocol with a maximum of 2 embryos transfer
IVFMD - MyDuc Hospital
Ho Chi Minh City, Vietnam
Number of metaphase II oocytes available after CAPA-IVM culture
This will be analyzed according to the patient's ovarian reserve
Time frame: 24-48 hours after eggs retrieved
Number of patients aspirated without oocytes
Count the number of patients aspirated without oocytes
Time frame: OR day
Number of patients without mature oocytes after CAPA-IVM
Count the number of patients without mature oocytes
Time frame: OR day
Number of patients without embryos
Count the number of patients without embryos
Time frame: OR day
Oocyte maturation rate
The oocyte maturation rate is calculated by dividing the number of MII oocytes after CAPA-IVM by the number of cumulus-oocyte complex (COC) retrieved
Time frame: 24-48 hours after eggs retrieval.
Fertilization rate
Number of fertilized oocytes divided by the number of ICSI oocytes
Time frame: ICSI day
Number of fertilized oocytes
Count the number of 2PN oocytes at 16-18 hours after ICSI
Time frame: 16-18 hours after ICSI
Number of day-3 embryos
Count the number of day-3 embryos at 64±2 hours after ICSI
Time frame: 64±2 hours after ICSI
Day-3 embryo rate
Number of day-3 embryos divided by the number of fertilized oocytes
Time frame: 64±2 hours after ICSI
Number of good quality day-3 embryos
Count the number of day-3 embryos graded as grade 1 and grade 2.
Time frame: 64±2 hours after ICSI
Number of day-3 embryos frozen
Count the number of day-3 embryos frozen
Time frame: 64±2 hours after ICSI
Number of day-5/6 embryos
Count the number of day-5 embryos at 114±2/140±2 after ICSI
Time frame: 114±2/140±2 after ICSI
Day-5/6 embryo rate
Number of day-5/6 embryos divided by the number of fertilized oocytes
Time frame: 114±2/140±2 after ICSI
Number of good quality day-5/6 embryos
Count the number of day-5/6 embryos graded as grade 1 and grade 2
Time frame: 114±2/140±2 after ICSI
Number of day-5/6 embryos frozen
Count the number of day-5/6 embryos frozen
Time frame: 114±2/140±2 after ICSI
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