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OpenTrials
Completed

NCT Number: NCT02145819

Optimal Planning of a Day 3 Cryopreserved(Frozen)-Thawed Embryo Transfer in a Natural Cycle With hCG Administration or After Spontaneous LH Peak?

The aim of the study is to determine whether spontaneous LH peak is superior to human chorionic gonadotropin before a transfer of a day 3 frozen embryo.

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Key information

Age range

18 year–39 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

Centre of Reproductive Medicine CRG

Jette, Brussels Capital, 1090, Belgium

About this study

For surplus embryos after fresh IVF-cycles, cryopreservation has become common medical practice. These frozen embryos are mostly replaced in an artificial cycle with exogenous estrogen and progesterone or in a natural cycle. Often, hCG is administered as an ovulation induction agent for scheduling purposes.

Successful implantation requires a co-ordinated series of events allowing a timely dialogue between a receptive endometrium and the intrusive blastocyst . The period of receptivity is thought to be 3 days in human. It is suggested that blastocyst apposition begins about day LH+6 and is completed by day LH+10

In general, the aim is to transfer the embryo during the 'window of implantation', what is defined as the period during which the uterus is receptive for implantation of the free-lying blastocyst. This has been a subject of debate since many years.

A prospective study by Fatemi et al. (2010) revealed a significantly higher ongoing pregnancy rate after transferring frozen-thawed embryos in natural cycles with a spontaneous LH peak compared with natural cycles controlled by hCG for final oocyte maturation and ovulation (31.1% vs. 14.3%, respectively). In this trial, FrET (frozen embryo transfer) was planned 5 days after the LH surge or 5 days after the administration of 5000IU of hCG.

In order to optimize the synchronization in the hCG group, and therefore enhance the pregnancy rates, the aim is to plan a FrET 6 days after hCG administration instead of 5 days. The rationale behind is that day 3 frozen embryos are thawed the day before embryo transfer, which means they are already at day 4 of the embryonic development.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Natural cycles, in which a frozen-thawed day 3 embryo is replaced.
  • Signed informed consent.
  • Regular cycle (i.e. between 26 and 35 days)
  • Normal transvaginal ultrasound at screening, without evidence of clinically significant abnormality consistent with finding adequate for ART with respect to uterus and adnexa.
  • Embryos frozen by vitrification.
  • Single or dual embryo transfer.

Exclusion criteria

  • Known allergic reactions to progesterone products.
  • Intake of experimental drug within 30 days prior to study start.
  • Contraindication for pregnancy.
  • Embryos of women above 39 years of age at the time of embryo freezing.
  • Recipients of oocyte donation cycles

Treatment and study plan

HCG

Drug

Other names: spontaneous LH peak

LH peak

Other

Primary outcomes

  1. clinical pregnancy rate

    Time frame: 7 weeks

    We evaluate the pregnancy, at 7 weeks amenorrhoea. Outcome is clinical pregnancy rate

Secondary outcomes

  1. number of monitoring visits at the clinic per cycle

    Time frame: 7 weeks

Sponsors and collaborators

Lead sponsor

Universitair Ziekenhuis Brussel

Other

Registry information

Acronym: PLUS

Important dates

Study start
2014
Primary completion
2019
Study completion
2019
First posted
May 23, 2014
Registry last updated
Sep 27, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.