Prospective Monitoring of Children Born in Haute Vienne From Uterine Life to Adulthood

Child Development Clinical Trial

— NEHAVI  

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02674087
• Other study ID #: I1 029
• Status: Recruiting
• Phase: N/A
• First received: April 14, 2014
• Last updated: February 3, 2016
• Start date: April 2014
• Est. completion date: April 2019

Study information

• Verified date: January 2016
• Source: University Hospital, Limoges
• Contact: Yves AUBARD, MD
• Phone: 05 55 05 61 07
• Email: yves.aubard[@]chu-limoges.fr
• Is FDA regulated: No
• Health authority: France: The Commission nationale de l’informatique et des libertés
• Study type: Observational [Patient Registry]

Clinical Trial Summary

The purpose of this survey is to collect data from intrauterine life until the age of 18 of children born in Haute Vienne.

The interest to realize such survey is to find correlations and interactions that may exist between the events that occurred during intrauterine life and those that will occur after the birth of the child. The investigators will examine every aspect of these children's lives from the perspectives of health, social sciences and environmental health

These are medical events (occurrence of disease, medication), but also socio-cultural for this child (living environment, exposure to possible contaminants, events in family history).

This cohort aims to include 3000 children a year (whose parents consented to their inclusion), all born at Haute-Vienne.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 9000
• Est. completion date: April 2019
• Est. primary completion date: April 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Any child born in one of the three maternity hospitals in the Haute-Vienne (CHU Limoges, Clinique des Emailleurs, Hospital Saint-Junien).

• Any child who's parents consented to their inclusion.

Exclusion Criteria:

• Children born at home.

• Children abandoned at birth.

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Child Development

Locations

Country	Name	City	State
France	Clinique des Emailleurs	Limoges
France	HME	Limoges
France	Centre Hositalier de Saint Junien	Saint Junien

Sponsors (4)

Lead Sponsor	Collaborator
University Hospital, Limoges	ARS, Fondation Patrtenariale Unilim, La poste

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of enrollment	3 years after the study has started, the investigators will evaluate the rate of enrollment.	At 3 years	No