Optimizing the Temperature for Embryo Culture in In Vitro Fertilization

Completed · Not applicable

Conditions studied: Infertility

In brief

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.

Key facts

Study ID: NCT01506089
Run by: Reproductive Medicine Associates of New Jersey
People needed: 55
Starts: 2012-01-01
Expected to finish: 2014-07-01
Last updated by the study team: 2015-03-26

Who can join

Age: 18 and older, up to 41. Sex: female. Healthy volunteers: accepted.

You may qualify if…

No more than 1 prior failed cycle at RMA NJ facility; up to 2 prior failed cycles at another facility pending investigator review
Female partner between 18 and 41 at onset of IVF cycle
Normal day 3 FSH (< or = 12) in RMA NJ laboratory
Basal antral follicle count of at least 10
Male partner with greater than 100,000 total motile spermatozoa per ejaculate (donor sperm is ok)
BMI < or = 32 kg/m2

You may not qualify if…

Diagnosis of chronic anovulation (cycles occuring typically less often than every 90 days)
Use of testicular aspiration or biopsy procedures to obtain sperm
Unevaluated ovarian mass or diagnosis of surgically-confirmed stage IV endometriosis
Presence of hydrosalpinges that communicate with the uterine cavity
History of endometrial insufficiency
Any contraindication to undergoing IVF or gonadotropin stimulation
Prior poor fertilization rate- less than 50% of mature eggs
Prior poor blastulation rate- less than 10% of 2PNs (day 1 embryos)

Where it is running

Reproductive Medicine Associates of New Jersey — Morristown, New Jersey, United States
Reproductive Medicine Associates of Pennsylvannia — Allentown, Pennsylvania, United States

Full record on ClinicalTrials.gov

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