Gonadotropin-releasing hormone agonist trigger in oocyte donors co-treated with a gonadotropin-releasing hormone antagonist: a dose-finding study

Fertil Steril. 2016 Feb;105(2):356-63. doi: 10.1016/j.fertnstert.2015.10.014. Epub 2015 Oct 31.

Abstract

Objective: To determine the optimal GnRH agonist dose for triggering of oocyte maturation in oocyte donors.

Design: Single-center, randomized, parallel, investigator-blinded trial.

Setting: IVFMD, My Duc Hospital, Ho Chi Minh City, Vietnam.

Patient(s): One hundred sixty-five oocyte donors (aged 18-35 years, body mass index [BMI] <28 kg/m(2), antimüllerian hormone level >1.25 ng/mL, and antral follicle count ≥6).

Intervention(s): Ovulation trigger with 0.2, 0.3, or 0.4 mg triptorelin in a GnRH antagonist cycle.

Main outcome measure(s): The primary end point was number of metaphase II oocytes. Secondary end points were fertilization and cleavage rates, number of embryos and top-quality embryos, steroid levels, ovarian volume, and ongoing pregnancy rate (PR) in recipients.

Result(s): There were no significant differences between the triptorelin 0.2, 0.3, and 0.4 mg trigger groups with respect to number of metaphase II oocytes (16.0 ± 8.5, 15.9 ± 7.8, and 14.7 ± 8.4, respectively), embryos (13.2 ± 7.8, 11.7 ± 6.9, 11.8 ± 7.0), and number of top-quality embryos (3.8 ± 2.9, 3.6 ± 3.0, 4.1 ± 3.0). Luteinizing hormone levels at 24 hours and 36 hours after trigger was significantly higher with triptorelin 0.4 mg versus 0.2 mg and 0.3 mg (9.8 ± 7.1 IU/L vs. 7.3 ± 4.1 IU/L and 7.2 ± 3.7 IU/L, respectively; 4.6 ± 3.2 IU/L vs. 3.2 ± 2.3 IU/L and 3.3 ± 2.1 IU/L, respectively. Progesterone level at oocyte pick-up +6 days was significantly higher in the 0.4-mg group (2.2 ± 3.7 ng/ml) versus 0.2 mg (1.1 ± 1.0 ng/ml) and 0.3 mg (1.2 ± 1.6 ng/ml). One patient developed early-onset severe ovarian hyperstimulation syndrome (OHSS).

Conclusion(s): No significant differences between triptorelin doses of 0.2, 0.3, and 0.4 mg used for ovulation trigger in oocyte donors were seen with regard to the number of mature oocytes and top-quality embryos.

Clinical trial registration number: NCT02208986.

Keywords: In vitro fertilization; dose-finding; gonadotropin-releasing hormone agonist trigger; oocyte donor; triptorelin.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Anti-Mullerian Hormone / blood
  • Drug Dosage Calculations
  • Embryo Transfer
  • Female
  • Fertility
  • Fertility Agents, Female / administration & dosage*
  • Fertility Agents, Female / adverse effects
  • Fertilization in Vitro
  • Gonadotropin-Releasing Hormone / administration & dosage
  • Gonadotropin-Releasing Hormone / adverse effects
  • Gonadotropin-Releasing Hormone / agonists*
  • Gonadotropin-Releasing Hormone / analogs & derivatives*
  • Gonadotropin-Releasing Hormone / antagonists & inhibitors*
  • Hormone Antagonists / administration & dosage*
  • Hormone Antagonists / adverse effects
  • Humans
  • Infertility / diagnosis
  • Infertility / physiopathology
  • Infertility / therapy*
  • Luteinizing Hormone / blood
  • Metaphase / drug effects
  • Oocyte Donation*
  • Oocytes / cytology
  • Oocytes / drug effects*
  • Oocytes / metabolism
  • Ovulation / drug effects
  • Ovulation Induction / adverse effects
  • Ovulation Induction / methods*
  • Pregnancy
  • Pregnancy Rate
  • Progesterone / blood
  • Treatment Outcome
  • Triptorelin Pamoate / administration & dosage*
  • Triptorelin Pamoate / adverse effects
  • Vietnam
  • Young Adult

Substances

  • Fertility Agents, Female
  • Hormone Antagonists
  • Triptorelin Pamoate
  • Gonadotropin-Releasing Hormone
  • Progesterone
  • Anti-Mullerian Hormone
  • Luteinizing Hormone
  • ganirelix

Associated data

  • ClinicalTrials.gov/NCT02208986