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Updated: Jul 25, 2025

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Published on: June 14, 2020
Does dual trigger improve euploidy rate in normoresponder? A cross-sectional study
Sule Yildirim Kopuk1, Zeynep Ece Utkan Korun1, Aysen Yuceturk1
1Acibadem Maslak Hospital, Assisted Reproductive Technologies Unit, Istanbul, Turkey.
Dual triggering using gonadotropin-releasing hormone (GnRH) agonist and hCG did not improve embryo euploidy rates in women undergoing in vitro fertilization. This study found no significant difference in euploidy rates between dual trigger and hCG-only trigger groups for normoresponders.
Area of Science:
- Reproductive Endocrinology
- In Vitro Fertilization
- Human Embryology
Background:
- Dual triggering, combining gonadotropin-releasing hormone (GnRH) analog and human chorionic gonadotropin (hCG), has shown promise for specific patient groups.
- Previous research indicated benefits for women with low mature oocyte yield or empty follicle syndrome.
Purpose of the Study:
- To evaluate the impact of dual triggering (hCG + GnRH agonist) on embryo euploidy rates.
- To determine if dual triggering improves in vitro fertilization outcomes in normoresponder women.
Main Methods:
- A cross-sectional study included 494 normoresponder women undergoing controlled ovarian stimulation.
- Participants were divided into two groups: hCG trigger (n=274) and dual trigger (hCG+GnRHa, n=220).
- Preimplantation genetic testing for aneuploidy (PGT-A) was performed on all biopsied embryos.
Main Results:
- A total of 1504 embryos were biopsied (881 in hCG group, 623 in dual trigger group).
- Euploidy rates were 35.4% in the hCG group and 29.8% in the dual trigger group.
- The hCG group showed a numerically higher euploidy rate per biopsied embryo (31.4% vs 26.5%), but the difference was not statistically significant (p > 0.05).
Conclusions:
- Adding a GnRH agonist to hCG for final follicular maturation in normoresponders does not enhance embryo euploidy rates.
- Dual triggering did not demonstrate a significant improvement in euploidy rates compared to hCG alone in this population.
- Further research may be needed to identify specific patient subgroups who benefit from dual triggering.
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