CompletedPhase 3ACTRN12614000715673

Administering Gonadotrophin Releasing Hormone (GnRH) Agonists during the Luteal Phase in Artificial Cycle Frozen-Thawed Embryo Transfers

Effect of administering GnRH agonists during the luteal phase on ongoing pregnancy rate in women undergoing artificial cycle frozen-thawed embryo transfers


Sponsor

Hopital Femme Mere Enfant

Enrollment

220 participants

Start Date

Oct 1, 2012

Study Type

Interventional

Conditions

Summary

Administering Gonadotropin Releasing Hormone (GnRH) agonistes during the luteal phase on In Vitro Fertilization treatment showed an improvement in pregnacy rate. The purpose of the study was to evaluate the effect of administering GnRH agonists during the luteal phase on ongoing pregnancy rate in women undergoing artificial cycle frozen-thawed embryo transfers.


Eligibility

Sex: FemalesMin Age: 18 YearssMax Age: 43 Yearss

Inclusion Criteria1

  • All patients undergoing artificial cycle of Frozen Thawed Embryo Transfers in our Assisted Reproduction Technology' s center

Exclusion Criteria1

  • Frozen Thawed Embryo Transfers resulting from oocyte or embryo donations

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Interventions

The aim of this study is to evaluate the benefit of - two sub cutaneous injections of GnRH agonists (tryptorelin 0.1 mg) administred on the 4th day and on the 6th day following the introduction of p

The aim of this study is to evaluate the benefit of - two sub cutaneous injections of GnRH agonists (tryptorelin 0.1 mg) administred on the 4th day and on the 6th day following the introduction of progesterone - In addition to usual progesterone supplementation (3 pills of 200 mg per day administred vaginally, 1 in the morning, 2 in the evening) The oestradiol supplementation was starded on the first day of the cycle : - From the first day to the 5th day of the cycle, they took 2 pills containing 2 mg of estradiol a day -From the 6th to the 10th day of the cycle, they took 3 pills containing 2 mg of estradiol a day. - They then took 4 pills containing 2 mg of estradiol a day until the pregnancy test. Oestrogen was first administered orally, then vaginally, following menstruation. Test were performed on the 13th day (blood test and ultrasonography). The progesterone was introduced when all conditions are met : The endometrium over 6 mm in thickness, pulsatility indexes below 3, and oestrogen levels above 750 pg/ml. If these conditions weren’t met, a 2nd test and up to a 3rd test were conducted, where oestrogen doses could be increased (increasing the dose to 5 or 6 pills a day). A pregnancy test (Human Chorionic Gonadotropin (HCG) assay) was conducted 16 days after the introduction of progesterone. Patients continued to take oestrogen and progesterone during the first three months of the pregnancy if this test was positive.


Locations(1)

Rhone Alpes, France

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ACTRN12614000715673