Assessing the Convenience of Natural Proliferative Phase Frozen Embryo Transfer

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-49
SponsorInstituto Valenciano de Infertilidade de Lisboa

About this trial

This study will assess the convenience of the natural proliferative phase frozen embryo transfer (NPP-FET) in terms of number of number of appointments needed before cycle scheduling.

Eligibility criteria

Qualifiers

Endometrial thickness ≥ 7 mm on the day of starting progesterone-based luteal phase support (LPS)

Serum progesterone levels <1.5 ng/ml on the day of starting progesterone-based LPS

LPS with micronized progesterone 400mg b.i.d.

Regular cycles (>24 days, ≤ 38 days)

Disqualifiers

Use of exogenous ovarian stimulation during FET

Untreated hydrosalpinx, polyp, submucous myomas or severe adenomyosis

Recurrent pregnancy loss (≥ 3 previous pregnancy losses)

Recurrent implantation failure with embryos from oocyte donation (≥ 3 previous failed embryo transfers)

Trial design

Treatments tested in this trial

  • Natural proliferative phase frozen embryo transfer

Treatment groups

530 Participants
are divided into 2 treatment groups

Sponsors and collaborators