Replacement of Fresh Embryo Transfers (ETs) by Frozen Embryo Transfers (FETs) Using Vitrification

Sponsor
Yazd Research & Clinical Center for Infertility (Other)
Overall Status
Unknown status
CT.gov ID
NCT00823121
Collaborator
(none)
500
1
2
16
31.3

Study Details

Study Description

Brief Summary

Cryopreservation of all embryos and transferring them subsequently in assisted reproductive technology (ART) cycles to improve outcome.

Condition or Disease Intervention/Treatment Phase
  • Procedure: freezing embryos by vitrification
  • Procedure: fresh embryo transfers
  • Drug: buserelin
  • Drug: recombinant FSH
  • Drug: human chorionic gonadotropin (pregnyl)
Phase 1/Phase 2

Detailed Description

All patients in the initial cohort were treated with long protocol for ovarian stimulation. For pituitary down-regulation, patients were treated with daily administration of 0.5 mg buserelin (suprefact, Aventis, Frankfurt, Germany) from day 21 of menstrual cycle. Buserelin was reduced to 0.25 mg daily when ovaries were quiescent on ultrasound, and COH was initiated with recombinant FSH (Gonal F, Serono, Aubnne, Switzerland) 150 IU/day on day 2 of withdrawal bleeding. Serial ultrasound examinations and evaluation of serum E2 levels were used to assess ovarian response, and then gonadotropin dose adjustments were done as required. Human chorionic gonadotropin (pregnyl, Organon, Oss, the Netherlands ) 10,000 IU was administered when at least two follicles reached a mean diameter of 18 mm.

Oocyte retrieval was performed 34-36 hours after hCG administration and conventional insemination or ICSI was performed as clinically appropriate.

In 187 patients allocated to fresh ET group, ET were performed on the day 2. Embryos were transferred under ultrasound guidance, with a C.C.D. embryo transfer catheter (Laboratory C.C.D., Paris, France). Luteal support with progesterone in oil (Progesterone, Aburaihan Co., Tehran, Iran) 100 mg daily IM was started on the day of oocyte retrieval and continued until the documentation of fetal heart activity on ultrasound.

In 187 patients allocated to FET group, cryopreservation of all embryos were undertaken with vitrification by Cryotop method and after two months, embryos were transferred.

The protocol for the Cryotop vitrification of embryos was described previously (Kuwayama et al., 2005; Kuwayama, 2007).

After a two-step loading with equilibration solution containing 7.5% (v/v) ethylene glycol and 7.5% (v/v) dimethyl sulfoxide, and vitrification solution containing 15% (v/v) ethylene glycol, 15% (v/v) dimethyl sulfoxide and 0.5 mol/L sucrose, embryos were loaded with a narrow glass capillary onto the Cryotop in a volume of < 0.1 µL . After loading, almost all the solution was removed to leave only a thin layer covering the embryos, and the sample was quickly immersed into liquid nitrogen (LN). Subsequently, the plastic cap was pulled over the film part of the Cryotop, and the sample was stored under LN. At warming, the protective cap was removed from the Cryotop while it was still submerged in LN and the Cryotop was immersed directly into a 37˚C medium containing sucrose. The embryos were then sequentially incubated in diluents solution before further in vitro culture for transfer.

Patients were prepared for ET with oral E2 to attain endometrial thickness ≥ 8 mm and triple line pattern on ultrasound scans. At that time, patients were given 100 mg of IM progesterone in oil daily and ET was preformed three days later under abdominal ultrasound guidance as described earlier. Oral E2 and progesterone were continued until documentation of fetal heart activity by ultrasonography.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
500 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Can Fresh Embryo Transfers be Replaced by Cryopreserved-thawed Embryo Transfers in Assisted Reproductive Cycles?
Study Start Date :
Aug 1, 2008
Anticipated Primary Completion Date :
Feb 1, 2009
Anticipated Study Completion Date :
Dec 1, 2009

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: frozen-embryo transfer

In this group all embryos are cryopreserved and two months later embryo transfer will perform.

Procedure: freezing embryos by vitrification
vitrification by Cryotop method
Other Names:
  • cryopreservation of embryos
  • Drug: buserelin
    Daily administration of 500 µg subcutaneous buserelin from day 21 of menstrual cycle; reduce to 250 µg daily when ovarian suppression is confirmed.
    Other Names:
  • suprefact
  • Drug: recombinant FSH
    gonadotropin stimulation with rFSH 150 IU/day from day 2 of menstrual cycle
    Other Names:
  • Gonal F
  • Drug: human chorionic gonadotropin (pregnyl)
    hCG 10,000 IU is administered when at least 2 follicles reach a mean diameter of 18 mm.
    Other Names:
  • pregnyl
  • Active Comparator: fresh embryo transfer

    In this arm fresh embryo transfers are performed on day 2 or 3.

    Procedure: fresh embryo transfers
    fresh embryo transfers
    Other Names:
  • embryo transfer using fresh embryos
  • Drug: buserelin
    Daily administration of 500 µg subcutaneous buserelin from day 21 of menstrual cycle; reduce to 250 µg daily when ovarian suppression is confirmed.
    Other Names:
  • suprefact
  • Drug: recombinant FSH
    gonadotropin stimulation with rFSH 150 IU/day from day 2 of menstrual cycle
    Other Names:
  • Gonal F
  • Drug: human chorionic gonadotropin (pregnyl)
    hCG 10,000 IU is administered when at least 2 follicles reach a mean diameter of 18 mm.
    Other Names:
  • pregnyl
  • Outcome Measures

    Primary Outcome Measures

    1. implantation rate [4 weeks]

    Secondary Outcome Measures

    1. on going pregnancy rate [3 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 38 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • age < 38

    • normal day 3 FSH

    • classified as high risk for OHSS

    • has ≥ 15 follicles with a mean diameter ≥ 12 mm per each ovary

    • E2 levels on the day of hCG administration > 3000 pg/mL

    • undergoing her first assisted reproduction treatment cycle

    Exclusion Criteria:
    • who does not have good-quality embryos appropriate for cryopreservation

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 : Research and clinical center for infertility Yazd Iran, Islamic Republic of 8916877391

    Sponsors and Collaborators

    • Yazd Research & Clinical Center for Infertility

    Investigators

    • Principal Investigator: abbas aflatoonian, M.D., Research and Clinical Center for Infertility
    • Principal Investigator: homa oskouian, M.D., Research and Clinical Center for Infertility

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00823121
    Other Study ID Numbers:
    • 654YazdRCCI
    First Posted:
    Jan 15, 2009
    Last Update Posted:
    Jan 20, 2010
    Last Verified:
    Apr 1, 2009

    Study Results

    No Results Posted as of Jan 20, 2010