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GnRH Agonist for Dual Trigger in IVF and for Luteal Phase Support in FET

RecruitingPhase 3Ages 18 Years - 42 YearsFemaleThe University of Hong Kong
NCT04064840 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The objectives of this study are to compare the efficacy of the dual trigger group vs the hCG trigger group on the live birth rate in women undergoing IVF and the efficacy of the agonist in LP group vs the placebo group on the live birth rate in women undergoing FET.

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📋 Eligibility rules (as published)
IVF Inclusion criteria: \- Women aged \<43 years at the time of IVF treatment Exclusion criteria: * Preimplantation genetic diagnosis treatment * Use of donor oocytes or donor embryos * Hydrosalpinx shown on pelvic scanning and not surgically treated * Women at risk of OHSS FET Inclusion criteria: * Women aged \<43 years at the time of IVF treatment * Replacing early cleavage embryos or blastocysts after thawing * FET in natural cycles Exclusion criteria: * Frozen early cleavage embryos thawed and cultured to blastocysts prior to transfer as requested by the patient * Preimplantation genetic diagnosis treatment * Use of donor oocytes or donor embryos * Hydrosalpinx shown on pelvic scanning and not surgically treated
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What it tests

  • IVF: Decapeptyl and hCG
  • FET: Decapeptyl
  • IVF: hCG and normal saline
  • FET: Normal Saline
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Where

1 site
Department of Obstetrics and Gynaecology
Hong Kong, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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