Cohort Of DEafness-gene Screening

Active, not recruitingOBSERVATIONAL
Enrollment

35,920

Participants

Timeline

Start Date

January 1, 2016

Primary Completion Date

March 31, 2021

Study Completion Date

December 31, 2028

Conditions
Hearing Loss
Interventions
GENETIC

Genetic screening test (Deafness gene variant detection array kit)

Infant participants were screened for fifteen variants in four genes (i.e., GJB2, SLC26A4, MT-RNR1 and GJB3).

All Listed Sponsors
collaborator

Nantong Maternal and Child Health Care Hospital

UNKNOWN

lead

Affiliated Hospital of Nantong University

OTHER

NCT06133946 - Cohort Of DEafness-gene Screening | Biotech Hunter | Biotech Hunter