Circadian Variation in Serum-progesterone Levels Following Controlled Ovarian Hyperstimulation.

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02673034

Enrollment

Registered

2016-02-03

Start date

2014-12-31

Completion date

2016-01-31

Last updated

2017-10-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility

Brief summary

The aim of the study is to investigate the circadian variation in serum-progesterone in women undergoing controlled ovarian stimulation.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 40 Years

Healthy volunteers

Yes

Inclusion criteria

Women undergoing standard IVF/ICSI treatment.

Exclusion criteria

Previous participation in the study.

Design outcomes

Primary

Measure	Time frame
serum progesterone levels	12 hours

Secondary

Measure	Time frame
serum LH levels	12 hours
serum estradiol levels	12 hours
17-OH progesterone	12-hours

Countries

Denmark

Outcome results