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Dual trigger for final oocyte maturation in expected normal responders with a high immature oocyte rate: a randomized controlled trial

OBJECTIVE: To evaluate whether dual trigger could improve reproductive outcomes in women with low oocyte maturation rates compare to human chorionic gonadotropin (hCG) trigger. METHODS: This study included expected normal ovarian responders younger than 40 years old whose immature oocyte rate in the...

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Detalles Bibliográficos
Autores principales: Yan, Meng-Han, Sun, Zhen-Gao, Song, Jing-Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10585044/
https://www.ncbi.nlm.nih.gov/pubmed/37869157
http://dx.doi.org/10.3389/fmed.2023.1254982
Descripción
Sumario:OBJECTIVE: To evaluate whether dual trigger could improve reproductive outcomes in women with low oocyte maturation rates compare to human chorionic gonadotropin (hCG) trigger. METHODS: This study included expected normal ovarian responders younger than 40 years old whose immature oocyte rate in the previous cycle was more than 50% at the reproductive center from July 2021 to November 2022. A total of 73 patients were enrolled at trigger, including 34 in the hCG trigger group and 39 in the dual trigger group (co-administration of gonadotrophin releasing hormone (GnRH) agonist and hCG, 40 and 34 h prior to oocyte retrieval, respectively). The primary outcome was oocyte maturation rate. RESULTS: There was no significant difference in the number of oocytes retrieved between the two study groups, but the oocyte maturation rate was higher in dual trigger group (84.0% [14.0%] vs. 55.5% [19.8%], p < 0.001). Moreover, there were also higher cumulative pregnancy rate (69.4% vs. 40.0%, p = 0.035) and cumulative live birth rate (66.7% vs. 36.0%, p = 0.022) in dual trigger group. CONCLUSION: For normal responders with low oocyte maturation rates, the dual trigger may be more effective than the conventional hCG trigger. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov, identifier ChiCTR2100049292.