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Vestibulotoxicity in consequence of tobramycin therapy in cystic fibrosis patients

Vestibulotoxicity in consequence of tobramycin therapy in cystic fibrosis patients - vestibulotoxicity in cystic fibrosis patients

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON29992
Enrollment
40
Registered
2006-10-30
Start date
2006-11-01
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

damage of the inner ear disturbance of equilibrium

Interventions

None listed

Sponsors

HagaZiekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: cystic fibrosis patients currently known in the HAGA hospital who have been treated at least one time with intravenous tobramycin and with an audiogram in medical dossier

Exclusion criteria

Exclusion criteria: patients treated with other intravenous aminoglycoside therapy than tobramycine patients receiving intravenous aminoglycosides during investigation. patients with perforation of one of the tympanic membranes. patients with a radical cave.

Design outcomes

Primary

MeasureTime frame
Primary study parameter is formulated as whether there is damage to the vestibulum or there is not.

Secondary

MeasureTime frame
Secundary study parameter is formulated as whether there is disturbance of equilibrium due to damage of the vestibulum or there is not.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)