Veterinary MedicineGynecologyPharmacotherapyAssisted Reproductive TechnologiesEmbryo TransferReproductive MedicineGonadal HormonesLuteal Phase SupportOvarian StimulationPost-thaw Embryo TransferProgesterone TherapyEmbryo Transfer Outcome AssessmentFrozen-thawed Embryo DevelopmentFrozen-thawed Embryo TransferGnrh Agonist Luteal SupportGnrh AgonistsHuman Chorionic Gonadotropin SupportObstetric Outcomes After Frozen TransferReproductive Outcome Assessment
BACKGROUND: There is no doubt that luteal phase support is essential to enhance the reproductive outcome in IVF cycles. In addition to progesterone and human chorionic gonadotropin, several studies have described GnRH agonists as luteal phase support to improve implantation rate, pregnancy rate and live birth rate, whereas other studies showed dissimilar conclusions. All of these studies have been done in fresh IVF cycles. OBJECTIVE: To determine whether an additional GnRH agonist administered at the time of implantation for luteal phase support in frozen-thawed embryo transfer (FET) improves the embryo developmental potential. MATERIALS AND METHODS: This is a prospective controlled trial study in 200 FET cycles, patients were randomized on the day of embryo transfer into group 1 (n=100) to whom a single dose of GnRH agonist (0.1 mg triptorelin) was administered three days after transfer and group 2 (n=100), who did not receive agonist. Both groups received daily vaginal progesterone suppositories plus estradiol valerate 6 mg daily. Primary outcome measure was clinical pregnancy rate. Secondary outcome measures were implantation rate, chemical, ongoing pregnancy rate and abortion rate. RESULTS: A total of 200 FET cycles were analyzed. Demographic data and embryo quality were comparable between two groups. No statistically significant difference in clinical and ongoing pregnancy rates was observed between the two groups (26% versus 21%, p=0.40 and 21% versus 17%, p=0.37, respectively). CONCLUSION: Administration of a subcutaneous GnRH agonist at the time of implantation does not increase clinical or ongoing pregnancy.
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Nicole G.M. Beckers, Nicholas S. Macklon, Marinus J.C. Eijkemans et al. · The Journal of Clinical Endocrinology & Metabolism · 2003 · 307 citations · Full text
Medicine, Endocrinology, Gynecology +15
Jan Tesařík, A. Hazout, Raquel Mendoza‐Tesarik et al. · Human Reproduction · 2006 · 158 citations