NCT02673034
Completed
Not Applicable
Circadian Variation in Serum-progesterone Levels Following Controlled Ovarian Hyperstimulation.
Regionshospitalet Viborg, Skive1 site in 1 country10 target enrollmentStarted: December 2014Last updated:
ConditionsInfertility
Overview
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Regionshospitalet Viborg, Skive
- Enrollment
- 10
- Locations
- 1
- Primary Endpoint
- serum progesterone levels
Overview
Brief Summary
The aim of the study is to investigate the circadian variation in serum-progesterone in women undergoing controlled ovarian stimulation.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to 40 Years (Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Women undergoing standard IVF/ICSI treatment.
Exclusion Criteria
- •Previous participation in the study.
Outcomes
Primary Outcomes
serum progesterone levels
Time Frame: 12 hours
Secondary Outcomes
- 17-OH progesterone(12-hours)
- serum LH levels(12 hours)
- serum estradiol levels(12 hours)
Investigators
Peter Humaidan
Professor, DMSc
Regionshospitalet Viborg, Skive
Study Sites (1)
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