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Clinical Trials/NCT02673034
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

Sponsor
Regionshospitalet Viborg, Skive
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Peter Humaidan

Professor, DMSc

Regionshospitalet Viborg, Skive

Study Sites (1)

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