Intratympanic Steroid Treatment For The Prevention Of Inner Ear Toxicity Associated With Systemic Treatment With Cisplatin.

Sponsor
Ziv Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT01285674
Collaborator
(none)
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Study Details

Study Description

Brief Summary

In this study we will aim to determine if cisplatin ototoxicity can be prevented by intratympanic administration of corticosteroids.

Condition or Disease Intervention/Treatment Phase
  • Drug: Intra-tympanic Cisplatinum
N/A

Detailed Description

Cisplatin is a potent and widely used antineoplastic drug. Ototoxicity is a serious and dose-limiting side effect. The ototoxic effect of cisplatin is characterized by irreversible, progressive, bilateral, high-frequency, sensorineural hearing loss with tinnitus. 60-80% of patients treated show elevations of hearing thresholds and nearly 15% sustain significant hearing handicap. There are currently no clinical interventions that have been shown to prevent cisplatin ototoxicity in humans. Glucocorticoids have significant potential for otoprotection. Glucocorticoids are in use for treatment of a variety of cochlear disorders such as autoimmune inner ear disease, Meniere's disease and sudden sensorineural hearing loss. Intratympanic administration of drugs is a contemporary, safe method of locally treating inner ear disorders, allowing diffusion across the round window into the inner ear. This method achieves much higher steroid levels within the inner ear compared to oral or parenteral routes. Local administration prevents the common systemic side effects of steroids. Previous animal studies have shown protection against cisplatin-induced ototoxicity after intratympanic steroid injection. Asa far as we know, there are yet no studies in humans examining the otoprotective effect of intratympanic steroids in patients treated with cisplatin. In this study we will aim to determine if cisplatin ototoxicity can be prevented by intratympanic administration of corticosteroids.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
INTRATYMPANIC STEROID TREATMENT FOR THE PREVENTION OF INNER EAR TOXICITY ASSOCIATED WITH SYSTEMIC TREATMENT WITH CISPLATIN.
Study Start Date :
Jan 1, 2011
Anticipated Primary Completion Date :
Jan 1, 2012
Anticipated Study Completion Date :
Jan 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intra-tympanic steroid injection

Drug: Intra-tympanic Cisplatinum
Intra-tympanic injection (under local anesthesia) of 0.5cc Methylprednisolone 62.5mg/cc. One injection per ear before each of the 3 cisplatin treatments. After injection the patient will remain with the treated ear upwards for 20 minutes and will try to avoid swallowing as much as possible.

Outcome Measures

Primary Outcome Measures

  1. Post-Treatment change in hearing [approximately 1 month from 1st treatment]

    change in hearing as a result of cisplatin treatment as assessed by behavioural hearing test and otoacoustic emissions

Secondary Outcome Measures

  1. Tinnitus [1 month post-treatment]

    appearence or worsening of tinnitus as a result of cisplatin treatment

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • adults 18 years old at least who are candidates for Cisplatin treatment

  • agreement to participate in the study

  • have signed an informed consent.

Exclusion Criteria:
  • refusal to participate

  • steroid treatment during the past month

  • external or middle ear disease not enabling intratympanic treatment

  • inner ear disease causing hearing loss

  • severe hearing loss for any reason

  • conductive hearing loss

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ziv Medical Center Safed Israel 13100

Sponsors and Collaborators

  • Ziv Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT01285674
Other Study ID Numbers:
  • 0035-10-ZIV
First Posted:
Jan 28, 2011
Last Update Posted:
Jan 28, 2011
Last Verified:
Jan 1, 2011
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 28, 2011