The primary objective is to determine which follicle sizes generate the highest rate of euploid blastocysts.
The primary objective is to determine which follicle sizes generate the highest rate of euploid blastocysts. Secondary objectives to be analysed between the different follicle sizes: * The number of cumulus oocyte complexes (COCs) retrieved per aspirated follicle size * The number of mature oocytes per COC retrieved (maturation rate) * The number of normally fertilized oocytes per number of oocytes injected (fertilization rate) * Embryo development up to the blastocyst stage * Chromosomal status of the biopsied blastocysts * Pregnancy rates after euploid blastocyst transfer * Miscarriage rate after euploid blastocyst transfer Most of the studies that looked at the relation between the follicular size and the developmental competence of the corresponding oocyte analysed normal responders with an average age of 35 years and normal BMI levels. However, during the last decades, a clear shift appeared in the patient population that present themselves for a fertility treatment. With many women delaying childbirth, we do not yet know how these advanced maternal age women may benefit from early or late trigger or from different follicular sizes. Also, the rising prevalence of obesity may impact the follicular growth, which has not been analysed at the individual follicle size before. For the above described reasons, we believe that the analysis of individual follicles and the developmental competence of the obtained oocyte, may guide us to improve individualized stimulation protocols for different subtypes of infertile patients. To guide us in this individualized process, this initial pilot study will be performed in a population of normal responders and will later be expanded to an infertile population with different characteristics.
Study Type
OBSERVATIONAL
Enrollment
24
While for an OPU out of the study the follicles are aspirated without measuring their sizes, now the follicles will be measured before they are aspirated. The measurement of the follicles is a non- invasive measurement: as the OPU is always performed under vaginal echo-guidance, the follicles are visible on the screen connected to the vaginal echo probe. By measuring two dimensions of the follicle, an average follicle diameter is registered for that follicle
IVI Middle East Fertilty Clinic
Abu Dhabi, United Arab Emirates
Blastocyst ploidy outcome according to the follicular size at the OPU
Blastocyst ploidy is determined after biopsy of trophectoderm cells, taken from the blastocyst on day 5, 6 or 7 from development. A biopsy is only possible if an oocyte was retrieved from the follicle that was mature, normally fertilized and developed into a blastocyst of sufficient quality for biopsy). The following outcomes are possible: 1. Normal 2. Abnormal 3. Inconclusive/No result
Time frame: 2 months
Recovery rate
Number of COCs retrieved/ number of follicles aspirated
Time frame: 2 months
Maturate rate
\# of MII oocytes/ # of COCs retrieved
Time frame: 2 months
Fertilization potential ( normal and abnormal fertilization)
Normal fertilization is assessed by the presence of 2 pronuclei 16-20 hours post insemination. This is normal fertilization. Abnormal fertilization is a deviation from the presence of 2 pronuclei, this can be one or three or more.
Time frame: 2 months
Embryo development up to blastocyst stage
development of an embryo from day 0 to the blastocyst stage includes all developmental stages The embryo will make multiple divisions that will be recorded every day of development. It wll go from 1 cell, to 2 cells, 3 cells etc to be 8 cells on day 3 of development. On day 4, the morula will form and the embryo will start to compact, which is indicated as compacting or compacted. After this stage, we are around day 5 of development, the embryo will start to cavitate, this is the beginning of blastulation. Different stages are observed. Bl1: cavity is less than 50%, bl2: cavity is larger tan 50%, bl3: full blastocyst, bl4; expanded blastocyst, bl5: hatching balstocyst, bl6: hatched blastocyst, bl7: hatching through an artificail opening, bl8: collpased blastocyst. Blastocysts will be scored according to Gardner and Schoolcraft (1999).
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Time frame: 2 months
Embryo development in time lapse incubators
assessing all specific time points
Time frame: 2 months
Chromosomal status of biopsied embryos
Blastocysts of sufficient quality will undergo trophectoderm biopsy. These 4-8 cells that are taken from the embryo are genitically tested for their chromosomal copy number. This will give an indication on the genetic status of the embryo. The embryo will be euploid if 23 pairs of intact chromosomes are present. If not, they are aneuploid.
Time frame: 2 months
mtDNA copy number
Mitoscore values is the ratio of the mitochondrial DNA over the nuclear DNA. This is presented as a value and has been linked to the implantation potential of the embryo. There is no unit.
Time frame: 2 months
Miscarriage rate after single euploid embryo transfer
loss of a pregnancy with hcg levels above 1000 IU after transfer
Time frame: 2 months
pregnancy rate after euploid embryo transfer
presence of bhCG above 15IU 12 days after transfer
Time frame: 2 months
biochemical pregnancy rate
characterized only by the presence of bhCG above 15 IU, no presence of gestational sac
Time frame: 2 months
clinical pregnancy rate
hCG \> 15 Iu/ml and ultrasound confirmation of a gestational sac
Time frame: 2 months
implantation rate
• Implantation rate calculated by the number of gestational sacs observed at echographic screening at 6 weeks of pregnancy divided by the number of embryos transferred, multiplied by 100.
Time frame: 2 months
ectopic pregnancy rate
where the embryo attached outside the uterus
Time frame: 2 months