Completed
CrèchMVEpidemiology of Human Cytomegalovirus Excretion in the Saliva of Children Attending Nursery in France.
What is being collected
Data Collection
Collected from today forward - ProspectiveDNA Samples
Who is being recruted
Infections
From 3 to 6 Years
+4 Eligibility Criteria
How is the trial designed
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Observational
Study Start: September 2009
Summary
Principal SponsorUniversity Hospital, Limoges
Last updated: November 1, 2013
Sourced from a government-validated database.Claim as a partner
Study start date: September 1, 2009
Actual date on which the first participant was enrolled.Salivary collection kit. 3 swab for DNA research, 1 for antibodies research and 1 for virus isolation by cell growth.
Principal SponsorUniversity Hospital, Limoges
Last updated: November 1, 2013
Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
2001 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Conditions
Criteria
Any sex
Biological sex of participants that are eligible to enroll.From 3 to 6 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Infections
Criteria
1 inclusion criteria required to participate
Children older than 3 months and less than 6 years kept in nurseries retained, regardless of the duration of custody of the child in the manger concerned
3 exclusion criteria prevent from participating
Refusal of parents (lack of consent)
Refusal of the child according to his ability to understand
Uninsured social security
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Treatment Groups
Study Objectives
One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
CompletedOne Study Center