NCT02673034

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Dec 2014

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2014

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2015

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2016

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

February 1, 2016

Completed
2 days until next milestone

First Posted

Study publicly available on registry

February 3, 2016

Completed
Last Updated

October 9, 2017

Status Verified

October 1, 2017

Enrollment Period

1 year

First QC Date

February 1, 2016

Last Update Submit

October 6, 2017

Conditions

Infertility

Outcome Measures

Primary Outcomes (1)

  • serum progesterone levels

    12 hours

Secondary Outcomes (3)

  • serum LH levels

    12 hours

  • serum estradiol levels

    12 hours

  • 17-OH progesterone

    12-hours

Eligibility Criteria

Age18 Years - 40 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

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

You may qualify if:

  • Women undergoing standard IVF/ICSI treatment.

You may not qualify if:

  • Previous participation in the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Fertility Clinic Skive

Skive, Resenvej 25, 7800, Denmark

Location

Biospecimen

Retention: SAMPLES WITHOUT DNA

Serum

MeSH Terms

Conditions

Infertility

Condition Hierarchy (Ancestors)

Genital DiseasesUrogenital Diseases

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor, DMSc

Study Record Dates

First Submitted

February 1, 2016

First Posted

February 3, 2016

Study Start

December 1, 2014

Primary Completion

December 1, 2015

Study Completion

January 1, 2016

Last Updated

October 9, 2017

Record last verified: 2017-10

Data Sharing

IPD Sharing
Will not share

Locations

DK(1)