Single Dose Gonadotropin-releasing Hormone (GnRH) Agonist Administration in the Luteal Phase of GnRH Antagonist Stimulated ICSI-ET Cycles

Last updated: November 3, 2009
Sponsor: V.K.V. American Hospital, Istanbul
Overall Status: Terminated

Phase

3

Condition

Infertility

Treatment

N/A

Clinical Study ID

NCT01007851
AH-48/07
  • Ages 18-45
  • Female

Study Summary

GnRH agonist administration in the luteal phase was reported to beneficially affect clinical outcome of ICSI-ET cycles. This randomized controlled trial evaluates the effect of a single dose GnRH agonist administered in the luteal phase on the outcome of ICSI - ET cycles stimulated with the fixed GnRH antagonist protocol. Women undergoing embryo transfer following controlled ovarian hyperstimulation with a fixed GnRH antagonist protocol were included. In addition to routine luteal phase support with progesterone women were randomized to receive a single dose of GnRH agonist or placebo on the sixth day after ICSI.Ongoing pregnancy rate was the primary outcome measure.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Women undergoing embryo transfer following controlled ovarian hyperstimulation with afixed GnRH antagonist protocol, oocyte pick-up and ICSI.

  • Embryo transfer performed on day 3

Exclusion

Exclusion Criteria:

  • Participation in another trial that was being conducted in our unit at the same time.

  • Preimplantation genetic screening cycles.

  • Day 5 embryo transfers.

Study Design

Study Start date:
September 01, 2006
Estimated Completion Date:
December 31, 2007

Connect with a study center

  • American Hospital

    Istanbul, 34365
    Turkey

    Site Not Available

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