Status:

COMPLETED

Progesterone Levels and Clinical Outcomes Using a Single Pessary of 400 mg of Vaginal Progesterone in Substitutive Cycles for Embryo Transfer.

Lead Sponsor:

Instituto Bernabeu

Conditions:

Luteal Phase Defect

Eligibility:

FEMALE

18-50 years

Brief Summary

This study aims to compare the efficacy, in terms of progesterone levels and clinical outcomes, of two different presentations of micronized vaginal progesterone (400 mg vs. 200 mg) used in endometria...

Eligibility Criteria

Inclusion

  • Patients with primary or secondary infertility undergoing endometrial preparation for an embryo transfer using standard doses of oral or transdermal estrogens.
  • Age between 18 and 50 years.
  • Normal uterine cavity verified by imaging techniques.
  • Serum progesterone documented on the day of embryo transfer.

Exclusion

  • Patients with a history of endometritis.
  • Patients diagnosed with Asherman's syndrome.
  • Patients with a different supplementation regimen or doses than those of the study groups.

Key Trial Info

Start Date :

March 3 2021

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

March 17 2021

Estimated Enrollment :

347 Patients enrolled

Trial Details

Trial ID

NCT04722471

Start Date

March 3 2021

End Date

March 17 2021

Last Update

March 19 2021

Active Locations (1)

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1

Instituto Bernabeu

Alicante, Valencia, Spain, 03016

Progesterone Levels and Clinical Outcomes Using a Single Pessary of 400 mg of Vaginal Progesterone in Substitutive Cycles for Embryo Transfer. | DecenTrialz