Progesterone Variation on the Final Day of Oocyte Maturation.

I

Institut Universitari Dexeus

Status

Completed

Conditions

Controlled Ovarian Stimulation
Circadian Rhythm
Progesterone Variation on Trigger Day
Oocyte Donors

Treatments

Diagnostic Test: Serum progesterone measure

Study type

Observational

Funder types

Other

Identifiers

NCT03366025
SMD-VPD-2017-03

Details and patient eligibility

About

The current study, aims through a robust design to provide a simple answer on whether progesterone levels of the same individual may significantly vary depending on the time of blood retrieval before the ovulation triggering, by evaluating the daily variability of serum progesterone on the day of triggering in healthy women who perform a COS for oocyte donation, through multiple blood samplings.

Enrollment

22 patients

Sex

Female

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy oocyte donors according to spanish law for oocyte donation
  • Controlled ovarian stimulation following a flexible antagonist protocol and stimulation with recombinant Follicular stimulating hormone.
  • Informed consent signed

Exclusion criteria

Detection of luteinizing hormone surge before triggering

Trial design

22 participants in 1 patient group

Oocyte donors
Description:
Healthy oocyte donors undergoing ovarian stimulation with recombinant Follicular stimulating hormone
Treatment:
Diagnostic Test: Serum progesterone measure

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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