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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03898440
Other study ID # DAG (29BRC18.0067)
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 15, 2019
Est. completion date September 4, 2021

Study information

Verified date January 2021
Source University Hospital, Brest
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine a threshold value of fetal anogenital distance in 2D ultrasound to differentiate male fetuses from female fetuses, starting 18 weeks of gestation and until the due date. The study also evaluates the feasibility of the measure and its interobserver variability.


Description:

The anogenital distance of female newborns is shorter than that of male newborns. Urogenital disorders, such as hypospadias and micro-penis, are associated with a shorter anogenital distance. Anogenital distance is a good marker of fetal exposure to androgenic substances. Prenatal anogenital distance ultrasound measure can help the diagnosis in case of doubt about fetal sexual phenotype or in case of urogenital disorder suspicion (hypospadias or micropenis). Is the anogenital distance easy to make measure? Can this procedure be reproduced? What are the threshold values to determine fetal sex at each term of pregnancy?


Recruitment information / eligibility

Status Completed
Enrollment 318
Est. completion date September 4, 2021
Est. primary completion date September 4, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - pregnant woman - sonographic fetal follow up in Brest Hospital - term>18 weeks of gestation Exclusion Criteria: - No datation between 11 weeks of gestation and 13 weeks of gestation and 6 days by crown-rump length measurement - Minor - no consent - ultrasound performed by an operator without ultrasonography graduation

Study Design


Locations

Country Name City State
France CHRU de Brest (Morvan) Brest

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Brest

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary fetal anogenital distance The distance will be measured from the center of the anus to the posterior convergence of the fourchette in female fetuses and to the posterior base of the scrotum in male fetuses During fetal ultrasound exam
Secondary Interobserver variability reproducibility of the anogenital measure: the measure will be taken by two sonographers during the same exam During fetal ultrasound exam
Secondary Ano-genital distance in mm the measure is correctly performed and validated by an expert During fetal ultrasound exam
Secondary Estimated fetal weight Impact of estimated fetal weight and anogenital distance During fetal ultrasound exam
Secondary neonatal sex determination concordance of anogenital distance and neonatal sex determination During fetal ultrasound exam
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