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Transtympanic Ringer's Lactate for the Prevention of Cisplatin Ototoxicity

Primary Purpose

Hearing Loss

Status
Unknown status
Phase
Phase 1
Locations
Canada
Study Type
Interventional
Intervention
Ringer's Lactate (0.03% Ciprofloxacin)
Sponsored by
McGill University Health Centre/Research Institute of the McGill University Health Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hearing Loss focused on measuring Ringer's, lactate, cisplatin, ototoxicity, hearing loss

Eligibility Criteria

15 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients over the age of 14
  • Patients undergoing platinum based chemotherapy
  • Patients who agree to participate in the study

Exclusion Criteria:

  • Patients unable to provide consent
  • Patients with head and neck cancer
  • Patients undergoing radiation of the head and neck
  • Patients who develop a tympanic perforation
  • Patients with persistent otorrhea

Sites / Locations

  • Montreal General HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Ringer's Lactate

Arm Description

Each patient will act as their own control with one ear receiving treatment, and the contralateral ear acting as control.

Outcomes

Primary Outcome Measures

Audiogram
Pre-, mid-(if available) and post-chemotherapy treatment audiograms will be compared to determine changes in hearing from baseline and between ears. Hearing will also be assessed every six months after chemotherapy treatment for up to four years to determine possible long-term effects.

Secondary Outcome Measures

Otoacoustic Emissions
Distortion Product Otoacoustic Emissions will also be measured before and after chemotherapy treatment and compared to determine significance.

Full Information

First Posted
April 1, 2010
Last Updated
April 20, 2010
Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
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1. Study Identification

Unique Protocol Identification Number
NCT01108601
Brief Title
Transtympanic Ringer's Lactate for the Prevention of Cisplatin Ototoxicity
Official Title
Transtympanic Administration of Lactate: An Innovative Otoprotection for Patients Receiving Cisplatin or Carboplatin Chemotherapy
Study Type
Interventional

2. Study Status

Record Verification Date
April 2010
Overall Recruitment Status
Unknown status
Study Start Date
April 2008 (undefined)
Primary Completion Date
April 2011 (Anticipated)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Cisplatin and carboplatin induce ototoxicity manifested as sensorineural hearing loss, tinnitus, and/or vestibular disturbances. Ototoxicity is induced via damage to inner ear structures by reactive oxygen species. Previous animal studies demonstrated that transtympanic injection of Ringer's Lactate (RL) provided near complete otoprotective effect against cisplatin. The purpose of this study is to determine if transtympanic administration of Ringer's Lactate via a pressure equalising (PE) tube in patients undergoing platinum based chemotherapy treatment will prevent tinnitus, vestibular dysfunction and hearing loss especially at high frequencies. Pre- and post- chemotherapy treatment audiometry will be measured and statistically analysed for significance.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hearing Loss
Keywords
Ringer's, lactate, cisplatin, ototoxicity, hearing loss

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Ringer's Lactate
Arm Type
Other
Arm Description
Each patient will act as their own control with one ear receiving treatment, and the contralateral ear acting as control.
Intervention Type
Drug
Intervention Name(s)
Ringer's Lactate (0.03% Ciprofloxacin)
Intervention Description
For each patient, only one ear will receive the Ringer's Lactate solution. The other ear will act as a control. To ensure adequate delivery of the solution to the middle ear, a small pressure equalizing tube will be inserted under local anesthesia before commencement of chemotherapy treatment. The patient will be instructed to administer four drops of RL solution to the experimental ear twice a day during their chemotherapy treatment.
Primary Outcome Measure Information:
Title
Audiogram
Description
Pre-, mid-(if available) and post-chemotherapy treatment audiograms will be compared to determine changes in hearing from baseline and between ears. Hearing will also be assessed every six months after chemotherapy treatment for up to four years to determine possible long-term effects.
Time Frame
Before and after chemotherapy treatment
Secondary Outcome Measure Information:
Title
Otoacoustic Emissions
Description
Distortion Product Otoacoustic Emissions will also be measured before and after chemotherapy treatment and compared to determine significance.
Time Frame
Before and after chemotherapy treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients over the age of 14 Patients undergoing platinum based chemotherapy Patients who agree to participate in the study Exclusion Criteria: Patients unable to provide consent Patients with head and neck cancer Patients undergoing radiation of the head and neck Patients who develop a tympanic perforation Patients with persistent otorrhea
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Victoria Akinpelu
Phone
514-412-4400
Ext
22249
Email
victoriakinpelu@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sam J Daniel, MD
Organizational Affiliation
McGill University Health Centre/Research Institute of the McGill University Health Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Montreal General Hospital
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H3G 1A1
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Victoria Akinpelu

12. IPD Sharing Statement

Citations:
PubMed Identifier
15547419
Citation
Choe WT, Chinosornvatana N, Chang KW. Prevention of cisplatin ototoxicity using transtympanic N-acetylcysteine and lactate. Otol Neurotol. 2004 Nov;25(6):910-5. doi: 10.1097/00129492-200411000-00009.
Results Reference
background
Links:
URL
http://clinicaltrials.gov/ct2/show/NCT00584155?term=ringer%27s+lactate&rank=2
Description
Protection From Cisplatin Ototoxicity by Lactated Ringers

Learn more about this trial

Transtympanic Ringer's Lactate for the Prevention of Cisplatin Ototoxicity

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