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Prospective study - detecting incidence and recovery of impaired inner ear function with Gentamicin use

Prospective detection of vestibular abnormalities resulting from the administration of Gentamicin and documentation of their subsequent recovery.

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12612000689875
Enrollment
500
Registered
2012-06-27
Start date
2012-07-01
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Gentamicin can have toxic effects on the inner ear which lessen an individual’s sense of spatial orientation and balance. The aim of this study is to investigate the incidence of this form of toxicity, and to investigate to what extent recovery is possible. This is done by recording eye movements, which have characteristic properties when movement sensors in the inner ear are non-functional. This study will use video-oculography to enable an objective serial recording of the eye movement abnormality. In selected patients, the eye movements will be recorded over 6 months to observe recovery. This will provide information on how quickly the vestibular-ocular reflex (VOR) function recovers.

Interventions

Impairment of the vestibulo-ocular reflex following the administration of Gentamicin. This will be monitored daily, ideally pre-treatment, during the course of all IV treated patients with ANY dose of Gentamicin and at 7 days following completion of treatment. Recovery of any defecit will be monitored for up to 6 months in patients who show signs of impaired vestibular function.

Sponsors

Capital and Coast District Health Board (CCDHB)
Lead SponsorHospital

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Participants must: be able to give consent prior to or while being treated at Wellington Hospital or Hutt Valley Hospital. The only inclusion criteria at day 1 will be treatment or pending treatment with IV Gentamicin within 24 hrs of measurement of the VOR gain.

Exclusion criteria

Patients so unwell that they do not wish to have their head moved or who decline testing or who are regarded by the examiner as being too ill to adequately co-operate.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026