This study tests the hypothesis that controlled ovarian stimulation impairs endometrial receptivity in normal responders.
The purpose of this study is to determine if blastocyst transfers in cycles of post-thaw extended culture (PTEC) have different efficacy than transfers of fresh blastocysts in patients with expected normal response to ovarian stimulation. Multiple studies have found altered endometrial histology and gene expression following controlled ovarian stimulation. PTEC cycles require cryopreservation of the entire 2pn oocyte cohort in the prior cycle. Once thawed, the embryos are cultured to the blastocyst stage before transfer. In typical cycles using frozen-thawed embryos, many thawed embryos that appear to survive do not actually resume and continue development. PTEC ensures the transfer of embryos that resumed development and continued developing at least to the blastocyst stage (4-5 days post-thaw). The viability of a blastocyst in a PTEC cycle has been shown to be on par with that of a fresh blastocyst. Therefore, comparing outcomes of blastocyst transfers in PTEC cycles with that in fresh autologous cycles allows the potential endometrial impact of controlled ovarian stimulation to be assessed.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
100
Cohort cryopreserved as bipronuclear (2pn) oocytes, then thawed and cultured to the blastocyst stage before transfer to the uterus.
Fresh blastocyst transfer following cycle of controlled ovarian stimulation.
Fertility Center of Las Vegas
Las Vegas, Nevada, United States
Clinical pregnancy (fetal heartbeat observed on ultrasound at 7 weeks gestation)
Time frame: 7 weeks gestation
Ongoing pregnancy at 10 weeks gestation
Time frame: 10 weeks gestation
Implantation rate (ratio of the number of fetal heart tones to the number of transferred blastocysts)
Time frame: 7 weeks gestation
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