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

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

Completed

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Key information

Conditions

Infertility Genital Diseases Urogenital Diseases

Age range

18 year–40 year

Sex eligibility

Female

Study type

Observational

Primary location

The Fertility Clinic Skive

Skive, Resenvej 25, 7800, Denmark

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Women undergoing standard IVF/ICSI treatment.

Exclusion criteria

Previous participation in the study.

Treatment and study plan

Primary outcomes

serum progesterone levels

Time frame: 12 hours

Secondary outcomes

serum LH levels

Time frame: 12 hours
serum estradiol levels

Time frame: 12 hours
17-OH progesterone

Time frame: 12-hours

Sponsors and collaborators

Lead sponsor

Regionshospitalet Viborg, Skive

Other

Registry information

Important dates

Study start: 2014
Primary completion: 2015
Study completion: 2016
First posted: Feb 3, 2016
Registry last updated: Oct 9, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed