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Clinical Trials/NCT02674087
NCT02674087TerminatedNot Applicable

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

University Hospital, Limoges5 sites in 1 country9,000 target enrollmentStarted: April 1, 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Sponsor
Enrollment
9,000
Locations
5
Primary Endpoint
Rate of enrollment

Study Overview

Brief 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.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

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.

Outcomes

Primary Outcomes

Rate of enrollment

Time Frame: At 3 years

3 years after the study has started, the investigators will evaluate the rate of enrollment.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
University Hospital, Limoges
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (5)

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