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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02139423
Other study ID # CRC12025
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 22, 2014
Est. completion date October 19, 2020

Study information

Verified date September 2021
Source Assistance Publique - Hôpitaux de Paris
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Universal hearing screening at birth by use of otoacoustic emission (OAE) is now offered in most maternities in France to detect symptomatic hearing impairment at birth but screening of cCMV infection is not coupled with this screening. In this study, the feasibility of achieving before one month of age the diagnosis of congenital CMV diagnosis and as well as the confirmation of hearing loss in newborns who failed newborn hearing screening will be tested.


Description:

Congenital cytomegalovirus (cCMV) is the most frequent congenital infection in France. Around 90% of cCMV infected infants are asymptomatic at birth, of whom 7 to 20% develop sensorineural hearing loss (SNHL). cCMV explains at least 10% of all hearing loss cases in young children. Early antiviral treatment (implemented before 1 month of age) with ganciclovir or valganciclovir can improve hearing outcome. In the absence of universal screening, cCMV remains largely undetected because most infected neonates are asymptomatic or have non-specific symptoms. When symptoms become apparent or develop, it may be too late for confirmation that the infection is of congenital origin becausediagnosis of congenital infection is based on the detection of CMV in samples collected within 2 to 3 weeks after birth. The presence of CMV in samples collected after this time may represent postnatal infection which does not carry the risk of hearing loss or neurodevelopmental sequelae. Universal hearing screening at birth by use of otoacoustic emission (OAE) is now offered in most maternities in France to detect symptomatic hearing impairment at birth but screening of cCMV infection is not coupled with this screening. In this study, the feasibility of achieving before one month of age the diagnosis of congenital CMV diagnosis and as well as the confirmation of hearing loss in newborns who failed newborn hearing screening will be tested.


Recruitment information / eligibility

Status Completed
Enrollment 235
Est. completion date October 19, 2020
Est. primary completion date March 31, 2018
Accepts healthy volunteers No
Gender All
Age group N/A to 10 Days
Eligibility Inclusion Criteria: - All newborns who have failed universal newborn screening Exclusion Criteria: - Neonates whose mothers would object to the use of their child's medical data

Study Design


Related Conditions & MeSH terms


Intervention

Other:
CMV PCR


Locations

Country Name City State
France Necker-Enfants-Malades Paris

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of days necessary to obtain the result of cCMV infection diagnosis and the audiological result after formal assessment 1 month
Secondary Measurement of CMV by quantitative PCR correlation between the results obtained from saliva and from blood (isolated from Guthrie cards) 4 months
Secondary Number of children for whom the result of the formal audiological assessment has been obtained 4 months
Secondary Number of children with cCMV infection and confirmed hearing loss in whom antiviral therapy has been initiated within the first month of life 4 months
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