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Gentamicin, genetic variation and deafness in preterm children

Gentamicin, genetic variation and deafness in preterm children: a case-control study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN39982239
Enrollment
300
Registered
2014-02-18
Start date
2013-01-27
Completion date
Unknown
Last updated
2019-06-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hearing loss in preterm infants Ear, Nose and Throat Other specified hearing loss

Interventions

This is an observational study which will only involve saliva samples and access to medical notes. Children with hearing loss will be invited to participate by their audiological paediatrician
ex-preterm children with normal hearing will be invited by their neonatologist. Saliva samples will be taken from children in both groups for genetic analysis of m.1555A>G. Clinical data including inf

Sponsors

University College London - Institute of Child Health (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Cases: babies born at 31 weeks and 6 days gestational age or less with hearing loss, treated on a neonatal unit within Greater London between 01/01/2009 -? 31/12/2013 Controls: babies born at 31 weeks and 6 days gestational age or less with normal hearing, treated on a neonatal unit within Greater London between 01/01/2009 ?- 31/12/2013

Exclusion criteria

Exclusion criteria: Cases: no exclusion criteria Controls: missing data in medication records

Design outcomes

Secondary

MeasureTime frame
Gentamicin administration, measured using data from medical notes

Primary

MeasureTime frame
Prevalence of the m.1555A>G mutation, measured using saliva samples tested for the mutation by direct DNA sequencing

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026