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Comparison of the standard GnRH antagonist protocol and the luteal phase estradiol/GnRH antagonist priming protocol in poor ovarian responders

dc.contributor.authorMutlu, Mehmet Firat
dc.contributor.authorMutlu, Ilknur
dc.contributor.authorErdem, Mehmet
dc.contributor.authorGuler, Ismail
dc.contributor.authorErdem, Ahmet
dc.date.accessioned2026-10-09T21:52:38Z
dc.date.issued2017
dc.departmentYüksek İhtisas Üniversitesi
dc.description.abstractBackground/aim: The aim of the study was to compare the luteal estradiol patch/GnRH antagonists priming protocol (LPP) with the standard GnRH antagonist protocol in poor ovarian responders (PORs) in terms of the outcomes of in vitro fertilization (IVF) treatment Materials and methods: IVF outcomes of 265 cycles in 265 patients (106 in the LPP group, 159 in the standard GnRH antagonist group) were evaluated retrospectively. Results: Mean length of stimulation (11.4 +/- 2.7 vs. 10.0 +/- 2.7 days; P < 0.05) and the total gonadotropin dose (3403 +/- 1060 vs. 2984 +/- 1112) used were significantly greater in the LPP group than in the standard GnRH antagonist protocol group. The mean number of oocytes retrieved (3.5 +/- 2.6 vs. 3.7 +/- 2.8), the number of mature oocytes (2.8 +/- 2.2 vs. 2.6 +/- 2.2), fertilization rates (65% vs. 62%), the number of embryos transferred (1.6 +/- 0.6 vs. 1.7 +/- 0.6), and implantation rates (16% vs. 13%) were similar. The cancellation rate did not significantly differ between the groups (9.4% vs. 13.2%). There were no significant differences in the clinical pregnancy (11.3% vs. 13.2%) or live birth rates per patient (3.8% vs. 9.4%) and clinical pregnancy (18.8% vs. 22.6%) or live birth rates per embryo transfer (6.3% vs. 12.9%) between the groups. Conclusion: LPP does not improve IVF outcomes when compared with the standard GnRH antagonist protocol in PORs.
dc.identifier.doi10.3906/sag-1602-111
dc.identifier.endpage475
dc.identifier.issn1300-0144
dc.identifier.issn1303-6165
dc.identifier.issue2
dc.identifier.orcid0000-0002-8098-2483
dc.identifier.orcid0000-0001-9944-6894
dc.identifier.pmid28425233
dc.identifier.scopus2-s2.0-85018751796
dc.identifier.scopusqualityQ2
dc.identifier.startpage470
dc.identifier.urihttps://doi.org/10.3906/sag-1602-111
dc.identifier.urihttps://hdl.handle.net/20.500.12794/3944
dc.identifier.volume47
dc.identifier.wosWOS:000399829700016
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.indekslendigikaynak.digerScience Citation Index Expanded (SCI-EXPANDED)
dc.language.isoen
dc.publisherTubitak Scientific & Technological Research Council Turkey
dc.relation.ispartofTurkish Journal of Medical Sciences
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.relation.sdgGoal-03: Good Health and Well-Being
dc.relation.sdgGoal-05: Gender Equality
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260922
dc.subjectVitro Fertilization
dc.subjectPoor Ovarian Response
dc.subjectGnrh Antagonists
dc.subjectEstradiol
dc.titleComparison of the standard GnRH antagonist protocol and the luteal phase estradiol/GnRH antagonist priming protocol in poor ovarian responders
dc.typeArticle

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