Infertility Clinical Trial
Official title:
Optimizing the Temperature for Embryo Culture in In Vitro Fertilization: A Randomized Controlled Trial
Many human and animal studies over the past 40 years have revealed that ovaries and
Fallopian tubes have a lower temperature than core body temperature, especially around the
time of ovulation and early embryo development. Whether average core body temperature, 37
degrees Celsius, is ideal temperature for culture has not been prospectively evaluated. The
purpose of this study is to determine whether lowering the incubator temperature by 1 degree
Celsius will result in meaningful improvements in embryo development and pregnancy rates.
Patients participating in this study will undergo routine in vitro fertilization (IVF)
stimulation. Following egg retrieval, patients with at least 8 mature eggs will have those
eggs divided randomly into two groups. Both groups will then under ICSI (intra-cytoplasmic
sperm injection) to fertilize the eggs. The groups will randomly be assigned to control or
study condition. The control condition group will be cultured at 37 degrees Celsius, the
current standard of care. The study group will be cultured at 36 degrees Celsius. All other
culture conditions will be kept identical and embryos will be assessed on day 3 and day 5 of
development.
On day 5, all well-developed blastocysts will undergo biopsy for Comprehensive Chromosomal
Screening (CCS), which will evaluate the chromosomal normalcy of the embryo . Patients will
undergo transfer on the morning of day 6 and the highest quality, chromosomally normal
embryo from each group (the 36 degree cultured embryos and the 37 degree cultured embryos)
will be transferred. If only 1 embryo is available for transfer, the patient will have a
single embryo transfer.
All embryos available for cryopreservation will undergo biopsy for CCS before being frozen.
Some arrested embryos from each temperature group will also undergo genetic analysis to
evaluate chromosomal normalcy or mosaicism.
The female patient will undergo a blood draw at 9 weeks gestation and buccal swabs will be
obtained from the infant(s) after birth.
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label
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