Fetal Alcohol Syndrome (FAS) Clinical Trials

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In Utero Alcoholic Exposure: PlGF, Biomarker of Fetal Brain Lesions

Status: Recruiting
Location: See location...
Intervention Type: Behavioral, Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study aims to validate that PLGF is a biomarker of cerebral lesions and therefore of secondary developmental disorders and disabilities that will be best diagnosed at 2 and 6 years of age.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: t
View:

∙ Mother:

• Pregnant woman (monofetal or twin pregnancy, whatever the parity)

• Age\> or = to 18 years

• Person affiliated to a social security system

• Person who read and understood the information form and signed the consent form

‣ Alcohol exposure group Chronic consumption of at least 30 g of alcohol per week or acute consumption of binge drinking type during pregnancy (knowing that a unit of 10 g of pure alcohol corresponds to 25 cl of beer 4 ° 5, 10 cl of wine at 12 °, 3 cl of whiskey, 7 cl of Porto ...)

⁃ Control group No alcohol consumption during pregnancy

⁃ Child Informed parents and written consent signed by the father and mother for the child's participation in this research (unless one of the parents does not have parental authority)

Locations
Other Locations
France
UH ROUEN
RECRUITING
Rouen
Contact Information
Primary
POURCHER
cecile.pourcher@chu-rouen.fr
02 32 88 82 65
Backup
BLOT
julien.blot@chu-rouen.fr
02 32 88 82 65
Time Frame
Start Date: 2017-01-27
Estimated Completion Date: 2026-03-27
Participants
Target number of participants: 60
Treatments
Other: Alcoholic exposure group
Blood sample (mother) Cord blood sample Placenta sample ASQ parental questionnaire WPPSI - IV and NEPSY development scales Scale of Conners SCQ questionnaire
Other: Control
Blood sample (mother) Cord blood sample Placenta sample ASQ parental questionnaire WPPSI - IV and NEPSY development scales Scale of Conners SCQ questionnaire
Related Therapeutic Areas
Sponsors
Leads: University Hospital, Rouen

This content was sourced from clinicaltrials.gov