Oocyte in vitro maturation (IVM) is an artificial reproductive technologies (ART) in which cumulus-oocyte complex (COC) are collected at the immature germinal vesicle (GV) stage from unstimulated or FSH-primed ovaries and matured in vitro before fertilization. IVM has been proposed as a more patient-friendly ART alternative to conventional IVF. Contrary to IVF, IVM is the only ART method with no cases of OHSS reported. Hence, patients with PCOS represent the major target population for IVM treatment. In clinical practice of standard IVM, COCs are aspirated from unstimulated or mildly stimulated ovaries and rapidly removed from the meiotic-inhibiting influence of the follicle and the follicular fluid. Regardless of in vitro gonadotrophin treatment, oocytes mature spontaneously in vitro, hence undergoing meiotic resumption in the absence of the usual elaborate cascade of endocrine and paracrine molecular signals that induce maturation in vivo. As such, the maturation of oocytes by standard IVM techniques is an artefact that compromises subsequent oocyte developmental competence. Numbers of studies have been proposed to improve the efficiency of IVM system. Synchronization of meiotic and cytoplasmic maturation in antral oocytes arrested at the immature GV-stage remains a major challenge and is of fundamental importance for successful fertilization. High intra-oocyte levels of cyclic adenosine monophosphate (cAMP), is crucial to maintain the nearly fully-grown oocytes under meiotic arrest and to induce oocyte maturation. Research in animal models has indicated that a non-physiological drop of cAMP levels in the oocyte results in asynchronous nuclear and cytoplasmic maturation. Investigators have reported the development of a novel in vitro simulated sequential oocyte maturation system. Critical to success of the approach is a pre-IVM phase that generates a rapid increase in COC cAMP levels. Secondly, the system utilizes an extended IVM phase containing sufficient FSH to drive meiotic induction in the presence of a type-3 PDE inhibitor. The high levels of cAMP in the oocyte and the induced nature of oocyte maturation mimics some of the key, newly characterized molecular signals that occur during oocyte maturation in vivo. Technical and conceptual elements were first developed using mouse, bovine and human COCs. Investigators propose a randomized clinical trial to compare a novel sequential culture system with the traditional standard oocyte IVM system for PCOS patients.
A multi-center, prospective, randomized clinical trial will be conducted, of comparing sequential oocyte IVM system with traditional oocyte IVM system for high OHSS risk PCOS patients (AMH\>5.6ng/ml). The inclusion criteria will be infertile patients diagnosed by the Chinese PCOS criteria, aged below 35 years, and without other known factors interfere reproductive or metabolic functions. 300 PCOS patients will be included and randomized into either of two groups: group A will administrate sequential oocyte IVM system and group B will administrate traditional standard oocyte IVM system. The comparison will be made between groups, and both groups are conducted with the HMG administration and embryo vitrification freezing. The primary outcome of the study is live birth rate. The embryo development and pregnancy outcomes will be followed up and compared between groups.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
300
The immature oocytes will be cultured in sequential oocyte IVM medium 1 for 6 hours (37℃, 5% CO2). After flushed 3 times, COCs were removed into sequential oocyte IVM medium 2 for further cultivation.
intracytoplasmic sperm injection (ICSI)
Patients administrates oestrogen (Progynova) 3mg twice a day for 10 to 12 days. From the day when endometrium reach a thickness of 8 mm and above, luteal phase support will be given with 10 mg progesterone (Dydrogesterone Tablets,) triple per day and utrogestan (Laboratories Besins International, Paris, France) 0.2g triple per day, until 14 days after embryo transfer.
COCs were aspirated and the immature oocytes will be cultured in traditional standard oocyte IVM system (Sage). 30 and 44 hours after cultivation, the maturity of oocytes will be assessed.
The Sixth Affiliated Hospital, Sun Yat-Sen University
Guangzhou, Guangdong, China
Jiangsu Province Hospital
Nanjing, Jiangsu, China
Reproductive medical hospital affiliated to Shandong University
Jinan, Shandong, China
The First Affiliated Hospital of Wenzhou Medical University
Wenzhou, Zhejiang, China
Tenth People's Hospital of Tongji University
Shanghai, China
Clinical pregnancy rate
The fetal heart beat in an intrauterine gestational sac under ultrasound will be defined as clinical pregnancy.
Time frame: 7 weeks gestation
Oocyte maturation rate
Oocyte maturation rate (%): number of MII oocytes/ number of oocytes retrieved.
Time frame: 30 and 46 hours after oocyte retrieval
Fertilization rate
Fertilization rate (%): number of oocytes fertilized/ number of oocytes retrieved.
Time frame: 30 and 46 hours after oocyte retrieval
Cleavage rate
Cleavage rate (%): number of cleavages/ number of 2PN embryos.
Time frame: 24 hours after ICSI
Day 3 embryo rate
Day 3 embryo rate (%): number of Day 3 embryos / number of 2PN embryos.
Time frame: 72 hours after ICSI
Good quality embryo rate at cleavage-stage
Good quality embryo rate at cleavage-stage (%): number of good quality embryos at cleavage-stage / number of 2PN embryos.
Time frame: 72 hours after ICSI
Number of cycles with available embryo
Available embryos will be defined as three days after oocyte retrieval with containing more than 4 cells and grade 1 to 2 or containing 4 cells with a grade of 1.
Time frame: 72 hours after ICSI
Blastulation rate
Blastulation rate (%): number of blastocysts / number of 2PN embryos.
Time frame: 144 hours after ICSI
Biochemical pregnancy rate
A serum β-hCG level above 5 IU/L, which is performed 12 days after embryos transfer, will be defined as biochemical pregnancy.
Time frame: 4 weeks gestation
Implantation rate
The implantation rate will be defined as the number of gestational sacs seen on the ultrasound divided by the total number of embryos transferred.
Time frame: 7 weeks gestation
Miscarriage rate (at first trimester)
Miscarriage at first trimester will be defined by any positive pregnancy test that result in a loss of pregnancy before 12 weeks gestation.
Time frame: 28 weeks gestation in maximum
Cumulative pregnancy rate
Cumulative pregnancy rate will be defined as clinical pregnancies with intrauterine fetal heart beat detected divided by the number of retrieval cycles whose embryos are all transferred.
Time frame: 1-2year
Preterm birth rate
Preterm birth means the baby is born before the 37th week of pregnancy in China.
Time frame: 1-2year
Newborn birth weight
Newborn birth weight
Time frame: 1-2year
Neonatal complication rate
We will collect complications that occur in the neonate including admission to the neonatal intensive care unit (NICU), hospitalization, etc.
Time frame: within one month after labor
Live birth rate
Live birth rate(%): number of live birth/ transferred cycle.
Time frame: 1-2year
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