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Progesterone Variation on the Final Day of Oocyte Maturation.

NCT03366025 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 22

Last updated 2018-04-04

No results posted yet for this study

Summary

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.

Conditions

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

Interventions

DIAGNOSTIC_TEST

Serum progesterone measure

Serum Progesterone will be measured in all donors on the day triggering at 8:00 am, 12:00 p, 16:00 pm and 20:00 pm

Sponsors & Collaborators

  • Fundacion Dexeus

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-11-01
Primary Completion
2018-01-25
Completion
2018-01-25

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03366025 on ClinicalTrials.gov