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Trial registered on ANZCTR
Registration number
ACTRN12619000120178
Ethics application status
Approved
Date submitted
20/12/2018
Date registered
25/01/2019
Date last updated
25/01/2019
Date data sharing statement initially provided
25/01/2019
Date results provided
25/01/2019
Type of registration
Retrospectively registered
Titles & IDs
Public title
Randomised Placebo controlled trial on Systemic Steroids to protect the Inner ear during Cochlear Implant Surgery
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Scientific title
Randomised Placebo controlled trial on Systemic Steroids to protect the Inner ear during Cochlear Implant Surgery
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Secondary ID [1]
296922
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nil known
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Universal Trial Number (UTN)
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Trial acronym
CIP2
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Ear health
310874
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Condition category
Condition code
Ear
309546
309546
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0
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Deafness
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
a slow intravenous injection of Methylprednisolone 13.5mg/kg (1000mg total dose for an average body weight 75Kg) over 10 minutes will be infused through an intravenous cannula 60 minutes prior to surgery.
This procedure will be monitored by the clinical trial coordinator.
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Intervention code [1]
313194
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Treatment: Drugs
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Comparator / control treatment
a slow intravenous injection of saline (placebo) will be infused through an intravenous cannula 60 minutes prior to surgery.
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Preservation of hearing as assessed by audiometry based on pre and post operative hearing test results.
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Assessment method [1]
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Timepoint [1]
308497
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12 months post-surgery
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Secondary outcome [1]
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The effect of the intervention on cochlear implant electrode common ground and monopolar impedances.
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Assessment method [1]
365995
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Timepoint [1]
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3 and 12 months after intervention
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Secondary outcome [2]
365996
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Preservation of hearing as assessed by audiometry based on pre and post operative hearing test results.
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Assessment method [2]
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Timepoint [2]
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3 months post-intervention
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Eligibility
Key inclusion criteria
Aged between 18 & 80 years of age at time of inclusion into the trial
85dB or better pure tone threshold (dBnHL) at 500Hz
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Minimum age
18
Years
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Maximum age
80
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
1. Note medically suitable due to past history of psychosis (mental illness), poorly controlled Type I diabetes, or known adverse reaction to steroids
2. Patients with poorly controlled hypertension, poorly controlled Type II diabetes or active gastro-oesophageal reflux will require medical clearance from the Department of Anaesthesia, or the responsible anaesthetist. Note: such individuals will require medical stabilisation prior to being fit for anaesthesia, so it would be appropriate to determine trial suitability from the anaesthetist when the preoperative medical workup is being undertaken
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Study design
Purpose of the study
Prevention
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Blinding will be achieved by the Pharmacy Department at the RVEEH. Pharmacy department will allocate for patients via a systemic randomised process for each patient who has met essential criteria.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation using a randomisation table created by computer software ( with 50%/50% pick of therapeutic intervention and placebo).
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 1 / Phase 2
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
A 2 proportions test (using 2 binomial proportions) will be computed to compare the proportion of subjects with preserved hearing in the control and treatment groups. Hearing preservation will be defined as a drop in pure tone threshold of equal to 20 dB at 500Hz (i.e. post-operative minus preoperative pure tone thresholds equal to 20 dB). The null hypothesis is that the proportion of hearing preservation will be identical in the two groups of patients. A two-tailed two proportions test with an alpha of 0.05 will determine whether the null hypothesis can be rejected.
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Recruitment
Recruitment status
Active, not recruiting
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Date of first participant enrolment
Anticipated
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Actual
12/04/2011
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Date of last participant enrolment
Anticipated
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Actual
24/06/2016
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Date of last data collection
Anticipated
31/01/2019
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Actual
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Sample size
Target
108
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Accrual to date
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Final
108
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment hospital [1]
12775
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The Royal Victorian Eye and Ear Hospital - East Melbourne
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Recruitment postcode(s) [1]
25236
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3002 - East Melbourne
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Funding & Sponsors
Funding source category [1]
301492
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Government body
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Name [1]
301492
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National Health Medical Research Council
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Address [1]
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16 Marcus Clarke St, Canberra ACT 2601
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Country [1]
301492
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Australia
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Primary sponsor type
University
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Name
University of Melbourne
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Address
University of Melbourne
Parkville Victoria 3010
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Country
Australia
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Secondary sponsor category [1]
301505
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None
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Name [1]
301505
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Address [1]
301505
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Country [1]
301505
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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The Royal Victorian Eye and Ear Hospital Human Research and Ethics Committee
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Ethics committee address [1]
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32 Gisborne Street East Melbourne VIC 3001
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
302236
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Approval date [1]
302236
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22/04/2010
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Ethics approval number [1]
302236
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10/939H
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Summary
Brief summary
This study aims to determine whether steroid (medication) delivered directly through an intravenous cannula before cochlear implant operation will better protect ear function during and after the operation.
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Trial website
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Trial related presentations / publications
Presented at 2018 Australian Society of Otlaryngology Head and Neck Surgery Annual Scientific Meeting.
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Public notes
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Contacts
Principal investigator
Name
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Prof Stephen O'Leary
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Address
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Dept Surgery - Otolaryngology, University of Melbourne,
5th Floor, Peter Howson Wing
Royal Victoria Eye and Ear Hospital 32 Gisborne Street, East Melbourne Victoria 3001
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Country
89542
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Australia
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Phone
89542
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+613 99298366
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Fax
89542
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Email
89542
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[email protected]
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Contact person for public queries
Name
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Thilakavathi Chengodu
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Address
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Thili Chengodu
Dept Surgery - Otolaryngology, University of Melbourne,
5th Floor, Peter Howson Wing
Royal Victoria Eye and Ear Hospital 32 Gisborne Street, East Melbourne Victoria 3001
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Country
89543
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Australia
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Phone
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+61 399298293
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Fax
89543
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Email
89543
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[email protected]
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Contact person for scientific queries
Name
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Stephen O'Leary
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Address
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Dept Surgery - Otolaryngology, University of Melbourne,
5th Floor, Peter Howson Wing
Royal Victoria Eye and Ear Hospital 32 Gisborne Street, East Melbourne Victoria 3001
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Country
89544
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Australia
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Phone
89544
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+613 99298366
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Fax
89544
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Email
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Systemic methylprednisolone for hearing preservation during cochlear implant surgery: A double blinded placebo-controlled trial.
2021
https://dx.doi.org/10.1016/j.heares.2021.108224
N.B. These documents automatically identified may not have been verified by the study sponsor.
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