Publication:
Scheduling gnrh antagonist cycles by a short course of oral estradiol administration during early follicular phase: A comparative study with non-scheduled cycles

dc.contributor.buuauthorAslan, Kiper
dc.contributor.buuauthorASLAN, MÜNİR KİPER
dc.contributor.buuauthorUNCU, GÜRKAN
dc.contributor.buuauthorAvci, Berrin
dc.contributor.buuauthorAVCI, BERRİN
dc.contributor.buuauthorUncu, Gürkan
dc.contributor.buuauthorSaribal, Seda
dc.contributor.buuauthorAta, Barış
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Kadın Hastalıkları Anabilim Dalı.
dc.contributor.orcid0000-0002-9277-7735
dc.contributor.orcid0000-0003-1106-3747
dc.contributor.researcheridC-8049-2013
dc.contributor.researcheridAAT-3479-2021
dc.contributor.researcheridAER-7173-2022
dc.contributor.researcheridAAH-9694-2021
dc.contributor.researcheridABE-6685-2020
dc.date.accessioned2024-08-13T06:59:43Z
dc.date.available2024-08-13T06:59:43Z
dc.date.issued2015-06-01
dc.description.abstractThis hypothesis generating study investigated whether GnRH antagonist cycles can be scheduled by a short course of oral estradiol administration during the follicular phase without impairing treatment outcome. Thirty-five women who underwent follicular phase estrogen scheduling (ES) of GnRH antagonist cycles were retrospectively matched for age and number of prior failed cycles with 35 women who underwent unscheduled GnRH antagonist cycles. ES group was given 6 mg/day estradiol orally from cycle day 2 until (including) one day before the scheduled start of stimulation. Gonadotropins were started on cycle days 2-3 in the control group. Flexible GnRH antagonist protocol was employed in both groups. ES group received estradiol for a median of 5 days. Total gonadotropin consumption was similar but one more GnRH antagonist injection was required in the ES group. Endometrial thickness on the day of hCG injection was increased in the ES group (12 versus 10 mm, p<0.01). Number of oocytes, metaphase II oocytes and transferred embryos were similar. Embryo implantation rates were 44.8% versus 34.4% (p=0.3), and clinical pregnancy rates were 48.6% versus 37.1%, (p=0.33) in the ES and control groups, respectively. All women in the ES group had oocyte retrieval and embryo transfer within the desired period.
dc.identifier.doi10.3109/09513590.2015.1006189
dc.identifier.endpage468
dc.identifier.issn0951-3590
dc.identifier.issue6
dc.identifier.startpage465
dc.identifier.urihttps://doi.org/10.3109/09513590.2015.1006189
dc.identifier.urihttps://hdl.handle.net/11452/43959
dc.identifier.volume31
dc.identifier.wos000359888500011
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherTaylor & Francis Ltd
dc.relation.journalGynecological Endocrinology
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi
dc.subjectIn-vitro fertilization
dc.subjectRandomized controlled-trial
dc.subjectOrthodox jewish couples
dc.subjectContraceptive pretreatment
dc.subjectHormone
dc.subjectProtocol
dc.subjectIvf
dc.subjectEstrogen
dc.subjectIvf/icsi
dc.subjectPill
dc.subjectAssisted reproduction
dc.subjectCycle scheduling
dc.subjectEstradiol
dc.subjectGnrh antagonist
dc.subjectIn vitro fertilization
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectEndocrinology & metabolism
dc.subjectObstetrics & gynecology
dc.subjectEndocrinology & metabolism
dc.titleScheduling gnrh antagonist cycles by a short course of oral estradiol administration during early follicular phase: A comparative study with non-scheduled cycles
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublicatione229a4fc-e771-4f54-9347-b06f2b9a7ee9
relation.isAuthorOfPublication35987a89-5462-4a6b-8e8f-5c3a7aa6484e
relation.isAuthorOfPublication8561b7b7-73b2-4dec-a681-9fdc21582789
relation.isAuthorOfPublication.latestForDiscoverye229a4fc-e771-4f54-9347-b06f2b9a7ee9

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