Local Heat-Stress as a Mechanism of Hearing Preservation
Primary Purpose
Hearing Loss
Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
ICS AirCal3
Sponsored by

About this trial
This is an interventional prevention trial for Hearing Loss
Eligibility Criteria
Inclusion Criteria: Any patient undergoing total cisplatin in total doses > 100mg/m2. Written consent. Age > 19 years. Exclusion Criteria: Inability to tolerate the intervention Exposure to cisplatin treatment without intervention. Head and neck carcinoma Baseline asymmetric hearing loss. Pregnant or breastfeeding women.
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Heat-stress
Arm Description
Each participant will undergo a 30-minute heat stress to one randomized ear. The participant will be reclined and the hot air caloric at 50°C applied by a licensed, unblinded audiologist for 30 minutes.
Outcomes
Primary Outcome Measures
Audiometric Effect
Audiometric evaluation will serve as the primary measure of outcome.
Secondary Outcome Measures
Full Information
NCT ID
NCT02872844
First Posted
August 16, 2016
Last Updated
August 17, 2023
Sponsor
University of Nebraska
1. Study Identification
Unique Protocol Identification Number
NCT02872844
Brief Title
Local Heat-Stress as a Mechanism of Hearing Preservation
Official Title
Local Heat-Stress as a Mechanism of Hearing Preservation in Adults Treated With Cisplatin: A Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Withdrawn
Why Stopped
Investigator closed study-no accrual
Study Start Date
November 3, 2016 (Actual)
Primary Completion Date
December 13, 2018 (Actual)
Study Completion Date
December 13, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Nebraska
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This pilot study plans to determine whether or not local heat-stress as a mechanism can help to preserve hearing in adults treated with Cisplatin.
Detailed Description
Evidence from the laboratory over the past 10-15 years has demonstrated that heat stress to the ear is otoprotectant against a variety of insults. The strongest evidence supports heat-shock protein 70 (Hsp70) as a key facilitator in this protection. Hsp70 is well established as a cell stabilizer, especially for cells undergoing significant stress. Hsp70 has been shown to protect against cisplatin-induced ototoxicity. Induction of Hsp70 may be accomplished pharmacologically, by whole-body heat stress, or by local heat stress. A form of local heat-stress is already employed in the common clinical setting of the warm caloric. This vestibular test has been in place since the early 20th century with a variety of studies evaluating the patient vestibular response to a variety of times and temperatures. Current clinical practice recommends either water or air calorics of 45°C or 50°C (respectively) at 45-60 seconds.
Several studies have described administering prolonged caloric stimulation to individual subjects without ill effect. Patients are able to tolerate stimulation up to 60 minutes without intolerable nystagmus or vertiginous symptoms or significant injury. Thus, it is feasible to provide warm stimulus to the ear for the recommended time of 30 minutes at the recommended temperature of 50°C (air) without significant risk to the patient.
The purpose of this study is to evaluate the impact of heat stress to the inner ear as an otoprotectant intervention against cisplatin-induced hearing loss. Patients that meet inclusion criteria will be offered audiometric evaluation before each cisplatin treatment and at 1, 3, 6, and 12 months following their chemotherapy. Patients will undergo their heat-stress 5-7 hours prior to their cisplatin treatment. Patients will serve as their own controls with one ear randomly receiving treatment and the other not. The primary outcome will be audiometric testing. Blood samples will be collected for serum levels of Hsp70 as a secondary outcome. A sample size of 12 achieves 80% power to detect a 0.9 standard deviation difference between ears using a two-sided paired t-test at 0.05 significance level.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hearing Loss
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Heat-stress
Arm Type
Experimental
Arm Description
Each participant will undergo a 30-minute heat stress to one randomized ear. The participant will be reclined and the hot air caloric at 50°C applied by a licensed, unblinded audiologist for 30 minutes.
Intervention Type
Device
Intervention Name(s)
ICS AirCal3
Intervention Description
Each patient will undergo a 30-minute heat stress to one ear. For randomization, the left ear will be treated in patients with a registration number ending with an odd number and the right for even numbers. An ICS AirCal3 Research Strategy (Otometrics) system attached to an Intel Core 15vPro Thinkpad (IBM) laptop is used within the audiometry department of a separate outpatient clinic. The patients will be reclined and the hot air caloric at 50°C applied by a licensed, unblinded audiologist for 30 minutes. The patients will be allowed to fixate and use whatever means they prefer for entertainment during the intervention.
Primary Outcome Measure Information:
Title
Audiometric Effect
Description
Audiometric evaluation will serve as the primary measure of outcome.
Time Frame
One year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Any patient undergoing total cisplatin in total doses > 100mg/m2.
Written consent.
Age > 19 years.
Exclusion Criteria:
Inability to tolerate the intervention
Exposure to cisplatin treatment without intervention.
Head and neck carcinoma
Baseline asymmetric hearing loss.
Pregnant or breastfeeding women.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paul Judge, MD
Organizational Affiliation
University of Nebraska
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Local Heat-Stress as a Mechanism of Hearing Preservation
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