2013
DOI: 10.1093/humrep/det374
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Comparison of early versus late initiation of GnRH antagonist co-treatment for controlled ovarian stimulation in IVF: a randomized controlled trial

Abstract: www.clinicaltrials.gov, no. NCT00866034.

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Cited by 12 publications
(7 citation statements)
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“…The potential detrimental effect of the GnRH antagonist upon the developing embryo may be significantly diminished after 2 days of insemination. This could be the reason for a lack of any significant negative effect of GnRH antagonists on pregnancy and live birth outcome [26][27][28]. Based on the results in Table 3 and previous reports, early cleavage of the zygote is not a reliable predictor for pregnancy potential using the GnRH antagonist protocol.…”
Section: Discussionmentioning
confidence: 78%
“…The potential detrimental effect of the GnRH antagonist upon the developing embryo may be significantly diminished after 2 days of insemination. This could be the reason for a lack of any significant negative effect of GnRH antagonists on pregnancy and live birth outcome [26][27][28]. Based on the results in Table 3 and previous reports, early cleavage of the zygote is not a reliable predictor for pregnancy potential using the GnRH antagonist protocol.…”
Section: Discussionmentioning
confidence: 78%
“…3,4 A randomized controlled trial by Hamdine O et al on comparison of early versus late initiation of GnRH antagonist in elevated p group also demonstrated no statistically significant difference in ongoing pregnancy rate. 12 A prospective interventional study and systemic metaanalysis review by Hamdine and nicks et al found that early elevated progesterone levels were associated with lower ongoing pregnancy rate in GnRH antagonist but the result was not statistically significant. 13 No differential impact of early or late GnRH antagonist initiation on the effect of elevated or normal progesterone on ongoing pregnancy rate was observed.…”
Section: Discussionmentioning
confidence: 99%
“…Thus, the negative effects observed in this study might be associated to these facts and not necessarily be present in antagonist treatments that are scheduled using cycle programming that allows a planned treatment start or when antagonist initiation is determined by ultrasonographically estimated follicle size and estradiol levels. However, a previous randomized study supports that delaying the start of GnRH antagonist treatment may be equally effective as early initiation, making possible the programming of antagonist cycles as well .…”
Section: Discussionmentioning
confidence: 99%