CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 843 enrolled
Drug / intervention
No interventionother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01028365
NCT01028365N/ACompleted
CompareCT.gov

Time to Conceive: A Study of Fertility: Biomarkers of Fertility

University of North Carolina, Chapel Hill·observational·Posted Dec 9, 2009·Updated May 4, 2017

In Brief

An observational study evaluating No intervention for Healthy. Completed, enrolled 843 participants across 1 site.

Detailed Summary

The purpose of this research study is to learn a way to measure a person's fertility. After 1 year of trying, 1 out of every 7 women will not be pregnant. This is called infertility. This results in significant distress and anxiety. Infertility is common; however, the investigators have no markers to predict who will be infertile. For couples diagnosed with infertility, the investigators have used blood and urine hormone levels (follicle stimulating hormone (FSH), inhibin B, and antimullerian hormone (AMH)) to tell us who will get pregnant with fertility treatment. The investigators don't know if these hormone levels can predict if regular people trying to get pregnant will be able to get pregnant. This study will try to determine if these hormone levels can predict fertility and infertility.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy
CountriesUnited States
CollaboratorsEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Timeline

N/ACompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedDec 9, 2009
Enrollment StartApr 1, 2008
Primary CompletionDec 1, 2016
TodayJul 2, 2026
Enrollment to primary: 8.7 yearsPosted 16.6 years ago

Interventions

No interventionother

Study participants will not be asked to make any changes to their daily lifestyle or existing health care routine. Participants also will not be asked to take any medications or change their diet.