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WithdrawnNCT02382068Updated Nov 9, 2017

Dexamethasone in Preventing Hearing Loss in Patients Receiving Cisplatin

An interventional study of Dexamethasone and Placebo in Malignant Neoplasm and Ototoxicity, sponsored by Aaron Moberly. Withdrawn. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-11-09.

Sponsored by Aaron Moberly · Not applicable, Interventional, and Supportive care

Why this study was withdrawn
No patients were enrolled to trial
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Not applicable
Ages
18 Years and older
Sex
All
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Study summary

This randomized pilot clinical trial studies dexamethasone in preventing hearing loss in patients receiving cisplatin. Injecting a steroid, such as dexamethasone, behind the eardrum before chemotherapy may help protect against cisplatin-associated hearing loss.

Read the detailed description

PRIMARY OBJECTIVES:

I. Investigate the potential protective effect of intratympanic dexamethasone administration on cisplatin-induced ototoxicity.

OUTLINE: Patients are randomized as to which ear receives dexamethasone.

Patients receive dexamethasone via intratympanic injection in one ear and placebo via intratympanic injection in the other ear.

After completion of study treatment, patients are followed up before each cisplatin treatment and then at 1 and 3 months after the last cisplatin treatment.

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Conditions studied

  • Malignant Neoplasm
  • Ototoxicity
03

In context

Neoplasms

10,818 studies on the registry are indexed under Neoplasms; 2,324 are open to participants now.

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Lead sponsor

This is the only study on the registry with Aaron Moberly as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Planned cisplatin treatment restricted to the following treatment course criteria:

    • Dose: > 50 mg/m\^2
    • Frequency: every (q)3-q4 weeks
    • Cycles: 7 maximum

Exclusion criteria

Exclusion Criteria:

  • Previous cisplatin treatment
  • Previous or concurrent radiation treatment to the head and neck region
  • Previous or existing pathology of the external or middle ear which would preclude auditory testing and/or intratympanic dexamethasone delivery
  • Previous or existing pathology of the inner ear with or without hearing loss (i.e. sudden sensorineural hearing loss, Meniere's disease, inner ear disease)
  • Previous or existing pathology of the central nervous system with potential to impact auditory pathways (i.e. major head trauma, meningitis, encephalitis, , vestibular schwannoma)
  • Recent treatment within the last month
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Brain metastases

Cancer deposits in the brain from a cancer that started elsewhere in the body (CNS metastases include the spinal cord).

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Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Supportive care (intratympanic dexamethasone)

    Patients receive dexamethasone via intratympanic injection in one ear and placebo via intratympanic injection in the other ear. Cisplatin standard of care treatment.

    Drug: Dexamethasone · Other: Placebo · Drug: Cisplatin

Interventions

  • Given via intratympanic injection

    Also known as: DM

  • OtherPlacebo

    Given via intratympanic injection

    Also known as: PLCB

  • Standard of care treatment with the following treatment course criteria: 1. Dose: \> 50 mg/m2 2. Frequency: q3 -q4 weeks 3. Cycles: 7 maximum

    Also known as: Platinol

06

What researchers measure

Primary outcomes

  1. Change in score of pure tone audiometry of conventional and high-frequency ranges (hearing level decibels [dB] hearing level)

    Change score will be assessed comparing baseline testing (prior to first cisplatin treatment) and various monitoring intervals (prior to each successive cisplatin treatment and 1 month and 3 months following completion of cisplatin treatment). Analyzed using a repeated measures model and a multi-level model.

    Time frame: Baseline to up to 3 months after completion of cisplatin treatment

Secondary outcomes

  1. Change in score of distortion product otoacoustic emissions of conventional and high-frequency ranges (amplitude dB sound pressure level)

    Will be assessed comparing baseline testing (prior to first cisplatin treatment) and various monitoring intervals (prior to each successive cisplatin treatment and 1 months and 3 months following completion of cisplatin treatment). Analyzed using a repeated measures model and a multi-level model.

    Time frame: Baseline to up to 3 months after completion of cisplatin treatment

  2. Presence of ototoxicity as defined by the American Speech-Language Hearing Association (ASHA)

    Presence or absence of ototoxicity as defined by the ASHA standards for pure tone audiometry (20 dB or greater change at any one test frequency, 10 dB or greater change at any two test frequencies, or any change at any three test frequencies). Analyzed using a repeated measures model and a multi-level model.

    Time frame: Up to 3 months after completion of cisplatin treatment

07

Study locations

No study locations are listed for this record.

08

References and documents

Related links

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 9, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02382068
Lead sponsor
Aaron Moberly
Responsible party
Aaron Moberly (Principal Investigator, Ohio State University Comprehensive Cancer Center) — Sponsor-investigator
First posted
Mar 6, 2015
Start date
Aug 2014 (estimated)
Primary completion
Jul 2017 (estimated)
Completion
Jul 2017 (estimated)
Last update
Nov 9, 2017

Study contacts

Aaron Moberly, MD
principal investigator · Ohio State University Comprehensive Cancer Center

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Nov 2017. You cannot join it, but the record below documents what was studied.

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Discussion

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Studies of the drugs tested here: Dexamethasone · Cisplatin

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