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RECRUITINGNCT02171845

Mechanisms and Factors Responsible for the Inhibition of Transposons During Fetal Gonad Development in Humans

This is a single-centre study over 36 months for the inclusion of 30 patients. The selection and inclusion of patients will take place according to the criterion of Medical Termination of Pregnancy at...

Lead sponsor: Centre Hospitalier Universitaire Dijon•1 locations•View source on ClinicalTrials.gov

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Contacts

Patricia FAUQUE

CONTACT

3.80.29.50.31 patricia.fauque@chu-dijon.fr

Sponsors

Lead Sponsor

Centre Hospitalier Universitaire Dijon

Age

0 - 0 years

Sex

MALE

Healthy Volunteers

No

Inclusion Criteria

•Couple or mother who has provided written informed consent
•Foetus between 10 and 37 weeks of amenorrhea (WA)
•Male foetus
•Foetus obtained following medical termination of pregnancy or voluntary termination of pregnancy

Exclusion Criteria

•persons without national health insurance cover
•foetus presenting aneuploidy
•foetus presenting a malformation of the genital organs

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: July 8, 2022Terms

Trial snapshot

StatusRECRUITING

Phase—

Enrollment30

Start dateJan 2014

Last updatedJul 8, 2022

Condition

Medical Termination of Pregnancy Voluntary Termination of Pregnancy

Locations shown

CHU de DIJON

Dijon

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: July 8, 2022Data synced to Clareo: May 25, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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