Skip to content

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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02171845
Enrollment
30
Registered
2014-06-24
Start date
2014-01-29
Completion date
2027-01-31
Last updated
2022-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Medical Termination of Pregnancy, Voluntary Termination of Pregnancy

Keywords

Male foetuses of 10 to 37 weeks

Brief summary

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 4 different gestational ages (8-12 weeks of gestation (WG)), 13-16 WG, 17-23 WG and 25-35 WG. The tissue analysed will principally be the gonads, other somatic tissue will also be systematically harvested in parallel (liver and psoas muscle) for control purposes. The gonads will be subjected to molecular biology analyses destined to quantify the expression of transposons and their inhibitors.

Interventions

OTHERsurgical biopsies

Sponsors

Centre Hospitalier Universitaire Dijon
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
10 Weeks to 37 Weeks
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

Design outcomes

Primary

MeasureTime frame
Spatio-temporal analysis of the activity of TEs by RT-qPCR and immunostainingBaselines

Secondary

MeasureTime frame
Promoter methylation profile by pyrosequencingBaselines

Other

MeasureTime frame
Spatiotemporal analysis piARN way: RT qPCR, Small RNA Seq, and immunoprecipitation of proteins PIWIBaselines

Countries

France

Contacts

Primary ContactPatricia FAUQUE
patricia.fauque@chu-dijon.fr3.80.29.50.31

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026