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

October 6, 2017 updated by: Peter Humaidan, Regionshospitalet Viborg, Skive
The aim of the study is to investigate the circadian variation in serum-progesterone in women undergoing controlled ovarian stimulation.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

10

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Denmark
    • Resenvej 25
      • Skive, Resenvej 25, Denmark, 7800
        • The Fertility Clinic Skive

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 40 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Sampling Method

Probability Sample

Study Population

Women undergoing IVF-treatment using either GnRHa long protocol or GnRH antagoinst co-treatment.

Description

Inclusion Criteria:

Women undergoing standard IVF/ICSI treatment.

Exclusion Criteria:

Previous participation in the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
serum progesterone levels
Time Frame: 12 hours
12 hours

Secondary Outcome Measures

Outcome Measure
Time Frame
serum LH levels
Time Frame: 12 hours
12 hours
serum estradiol levels
Time Frame: 12 hours
12 hours
17-OH progesterone
Time Frame: 12-hours
12-hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Regionshospitalet Viborg, Skive

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2014

Primary Completion (Actual)

December 1, 2015

Study Completion (Actual)

January 1, 2016

Study Registration Dates

First Submitted

February 1, 2016

First Submitted That Met QC Criteria

February 1, 2016

First Posted (Estimate)

February 3, 2016

Study Record Updates

Last Update Posted (Actual)

October 9, 2017

Last Update Submitted That Met QC Criteria

October 6, 2017

Last Verified

October 1, 2017

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CirProg

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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