Cochlear ImplantIGCIP vs SOCNCT02815124
Trial of Image-Guided Cochlear Implant Programming Versus Standard of Care
A study testing Image-Guided Cochlear Implant Programming in people with Cochlear Implant, run by Vanderbilt University Medical Center at 1 site in United States.
Trial summary
Cochlear implants are surgically implanted devices which restore the ability to hear to the hearing impaired. While remarkably successful, even in the best of performers restoration of hearing to levels of normal listeners is unusual. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Cochlear Implant
- What is being tested?
- Image-Guided Cochlear Implant Programming
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 0 participants
- Where
- 1 siteUnited States
- Study dates
- Dec 2021to 31 Dec 2021
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Adults ≥ 18 years of age that have undergone diagnostic testing for sensorineural hearing loss and are candidates for cochlear implantation will be considered eligible for the study
Who cannot join
- Age < 18 years
- Pre-lingual onset of deafness
- Mini-Mental State Exam < 24 (to remove cognitive decline as a confounding variable)
- Congenital inner ear malformation as detected on pre-operative CT scan performed as routine care
- Non-English speaking (because our audiological speech testing battery is validated for English speakers)
- Have undergone cochlear implantation outside of the Vanderbilt system
- Pregnancy which is a contraindication for elective CT scanning and surgery
Trial locations and contacts
1 site in 1 country.
United States1 site
Vanderbilt University Medical Center
Nashville, Tennessee, 37232
About this study
Official title: Randomized Controlled Trial of Image-Guided Cochlear Implant Programming Versus Standard of Care
Cochlear implants are surgically implanted devices which restore the ability to hear to the hearing impaired. While remarkably successful, even in the best of performers restoration of hearing to levels of normal listeners is unusual. Approximately 3 weeks after surgery, cochlear implants are activated via mapping - a process in which each individual electrode (FDA approved cochlear implants have between 12 and 22 electrodes) is turned on and the stimulus level adjusted to a level that is comfortable and beneficial to the recipient. At present, this standard of care mapping procedure is performed without knowledge of the physical location between the cochlear implant electrodes and the neural interface. Our team has developed a new method of mapping using post-operative CT scans and image processing to specify the physical relationship between the cochlear implant electrodes and the neural interface allowing customized mapping. Using this information, the investigators deactivate sub-optimally positioned electrodes. The investigators term this "Image-guided Cochlear Implant Programming" (IGCIP). In a prospective fashion, the investigators have implemented IGCIP on cochlear implant recipients who have had at least 6 months of standard of care (SOC) mapping. The purpose of this study is to perform a randomized controlled trial (RCT) on newly activated cochlear implant recipients randomizing between IGCIP and SOC.
Read the detailed description
Over 320,000 individuals have received cochlear implants (CIs) to restore hearing to the hearing impaired. Commercially available CIs have 12, 16, or 22 independent electrodes (the # is dependent on the manufacturer of the CI) which cover the entire frequency spectrum of the cochlea from 20,000 Hertz (Hz) at the base of to 200Hz at the apex. After implantation, an audiologists individually adjusts stimulation levels of each electrode following which all electrodes are turned on such that the whole frequency spectrum of speech can be appreciated. This is known as "standard of care" (SOC) programming. While postoperative speech understanding is significantly better than preoperative levels, even the best performers complain that the fidelity of natural hearing is not reproduced. Additionally, a significant minority achieves poor outcomes despite normally functioning equipment for reasons that are unknown but likely relate to poor neural survival; however, this cannot be confirmed as post-mortem histopathology is required to accurately document spiral ganglion cell count.
In recent years much attention has focused on the interface between the cochlear implant electrodes and the auditory neurons they are stimulating. Technological improvements at Vanderbilt in imaging processing have made it possible to determine the location of each electrode array in relationship to the frequency spectrum of the cochlea.
Using this information, the investigators have developed a new method of CI programming which they call image-guided cochlear implant programming, or IGCIP in which sub-optimally placed electrodes are turned-off or deactivated. Sub-optimally placed electrodes are defined as ones for which their neighboring electrodes are in closer proximity to the site of their neural stimulation. By deactivating sub-optimally positioned electrodes, channel interaction is reduced allowing a cleaner signal to be presented to the auditory nerve.
The investigators have implemented this strategy on 133 CIs of post-lingually deafened (hearing loss after the ability to speak) adult CI users with median use of their CI's with SOC programming of 1.3 years (range 0.3-15.5). When trialing IGCIP, mean word scores increased from 48.8±23.7% to 53.3±22.8% correct, and mean sentence scores increased from 62.2±28.5% to 65.0±26.9% correct. Both of these finding were statistically significant. Extracting out the pre-lingually (hearing loss before the ability to speak) deafened adults, the investigators see that for word scores, 24 of the 133 (28%) had statistically significant improvement 12 of the 133 (9%) had statistically significant decline, and the remaining 97 (73%) had equivocal results. Similarly, for the sentence scores, 36 of the 133 (27%) had statistically significant improvement 24 of the 133 (18%) had statistically significant decline, and the remaining 73 (55%) had equivocal results.
Perhaps the most important metric is which map patients select for long term use - SOC or IGCIP. Ninety-six of the 133 (72.1%) participants elected to keep IGCIP for long term use despite prior research that shows that there is a bias for CI recipients to favor their original map over a new map. And, for the 28% for elected to keep their SOC map, the process involves no risk - the deactivated electrodes are simply reactivated. Given these exciting prospective findings, the investigators are now proposing a randomized controlled trial (RCT) for newly activated adult CI recipients with both the CI user and testing audiologist blinded as to program (SOC or IGCIP). The investigators hypothesize that CI recipients randomized to IGCIP will have improved hearing performance as assessed by both word and sentence testing.
- Conditions
- Cochlear Implant
- Being tested
- Standard of Care, Image-Guided Cochlear Implant Programming
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Standard of CareOther
Post Cochlear Implant surgery, subject will receive activation/programming of their implant using Standard of Care
Image-Guided Cochlear Implant ProgrammingOther
Post Cochlear Implant surgery, subject will receive activation/programming of their implant using Image-Guided Cochlear Implant Programming
| Study group | Role | What they receive |
|---|---|---|
| Standard of Care | Active comparator | Cochlear Implant programming using standard of care Receives: Other: Standard of Care |
| Image-Guided Cochlear Implant Programming | Experimental | Cochlear Implant programming using Image-Guided Cochlear Implant Programming Receives: Other: Image-Guided Cochlear Implant Programming |
What is being measured
The primary outcome is the main question the study is designed to answer.
AzBio Sentence Scores at +5 Signal to Noise Ratio (SNR)
Measured: Month 1 post cochlear implant activation
AzBio Sentence Scores at +5 Signal to Noise Ratio (SNR)
Measured: Month 3 post cochlear implant activation
AzBio Sentence Scores at +5 Signal to Noise Ratio (SNR)
Measured: Month 6 post cochlear implant activation
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Jun 2016 (estimated)
- Study startDec 2021 (estimated)
- Primary completionDec 2021 (estimated)
- Study completion31 Dec 2021
Why it stopped: No funding secured and staffing changes resulting in no personnel to assist with study tasks.
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cochlear ImplantStudies of the same condition, open and under way.
- More trials run by Vanderbilt University Medical CenterThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind
- Who is masked
- Participant, Care provider, Investigator
- Enrolment
- 0 participants (actual)
Sponsor and investigators
- Lead sponsor
- Vanderbilt University Medical Center
- Sponsor type
- University, hospital or other
- Collaborators
- National Institute on Deafness and Other Communication Disorders (NIDCD)
- Responsible party
- Principal investigator, Robert F. Labadie, Vanderbilt University Medical Center
- Investigators
- Robert F. Labadie, MD, PhD, Principal investigator, Vanderbilt University Medical CenterBenoit M. Dawant, PhD, Study chair, Vanderbilt University Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02815124
- Sponsor's protocol ID
- 160461
- Other IDs
- R01DC014462
- Acronym
- IGCIP vs SOC
- Status last verified
- Jan 2022
- First submitted
- 22 Jun 2016
- Last updated
- 20 Jan 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 20 Jan 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Randomized Controlled Trial of Image-Guided Cochlear Implant Programming Versus Standard of Care
- ClinicalTrials.gov ID
- NCT02815124
- Acronym / sponsor ID
- IGCIP vs SOC / 160461
- Conditions
- Cochlear Implant
- Study type
- Interventional
- Recruitment status
- WithdrawnReason stopped: No funding secured and staffing changes resulting in no personnel to assist with study tasks.
- Enrolment
- 0 participants (actual)
- Lead sponsor
- Vanderbilt University Medical CenterUniversity, hospital or other
- Collaborators
- National Institute on Deafness and Other Communication Disorders (NIDCD)
- Study start
- Dec 2021 (estimated)
- Primary completion
- Dec 2021 (estimated)
- Study completion
- 31 Dec 2021 (actual)
- First posted
- 28 Jun 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Cochlear implants are surgically implanted devices which restore the ability to hear to the hearing impaired. While remarkably successful, even in the best of performers restoration of hearing to levels of normal listeners is unusual. Approximately 3 weeks after surgery, cochlear implants are activated via mapping - a process in which each individual electrode (FDA approved cochlear implants have between 12 and 22 electrodes) is turned on and the stimulus level adjusted to a level that is comfortable and beneficial to the recipient. At present, this standard of care mapping procedure is performed without knowledge of the physical location between the cochlear implant electrodes and the neural interface. Our team has developed a new method of mapping using post-operative CT scans and image processing to specify the physical relationship between the cochlear implant electrodes and the neural interface allowing customized mapping. Using this information, the investigators deactivate sub-optimally positioned electrodes. The investigators term this "Image-guided Cochlear Implant Programming" (IGCIP). In a prospective fashion, the investigators have implemented IGCIP on cochlear implant recipients who have had at least 6 months of standard of care (SOC) mapping. The purpose of this study is to perform a randomized controlled trial (RCT) on newly activated cochlear implant recipients randomizing between IGCIP and SOC.
Detailed description
Over 320,000 individuals have received cochlear implants (CIs) to restore hearing to the hearing impaired. Commercially available CIs have 12, 16, or 22 independent electrodes (the # is dependent on the manufacturer of the CI) which cover the entire frequency spectrum of the cochlea from 20,000 Hertz (Hz) at the base of to 200Hz at the apex. After implantation, an audiologists individually adjusts stimulation levels of each electrode following which all electrodes are turned on such that the whole frequency spectrum of speech can be appreciated. This is known as "standard of care" (SOC) programming. While postoperative speech understanding is significantly better than preoperative levels, even the best performers complain that the fidelity of natural hearing is not reproduced. Additionally, a significant minority achieves poor outcomes despite normally functioning equipment for reasons that are unknown but likely relate to poor neural survival; however, this cannot be confirmed as post-mortem histopathology is required to accurately document spiral ganglion cell count.
In recent years much attention has focused on the interface between the cochlear implant electrodes and the auditory neurons they are stimulating. Technological improvements at Vanderbilt in imaging processing have made it possible to determine the location of each electrode array in relationship to the frequency spectrum of the cochlea.
Using this information, the investigators have developed a new method of CI programming which they call image-guided cochlear implant programming, or IGCIP in which sub-optimally placed electrodes are turned-off or deactivated. Sub-optimally placed electrodes are defined as ones for which their neighboring electrodes are in closer proximity to the site of their neural stimulation. By deactivating sub-optimally positioned electrodes, channel interaction is reduced allowing a cleaner signal to be presented to the auditory nerve.
The investigators have implemented this strategy on 133 CIs of post-lingually deafened (hearing loss after the ability to speak) adult CI users with median use of their CI's with SOC programming of 1.3 years (range 0.3-15.5). When trialing IGCIP, mean word scores increased from 48.8±23.7% to 53.3±22.8% correct, and mean sentence scores increased from 62.2±28.5% to 65.0±26.9% correct. Both of these finding were statistically significant. Extracting out the pre-lingually (hearing loss before the ability to speak) deafened adults, the investigators see that for word scores, 24 of the 133 (28%) had statistically significant improvement 12 of the 133 (9%) had statistically significant decline, and the remaining 97 (73%) had equivocal results. Similarly, for the sentence scores, 36 of the 133 (27%) had statistically significant improvement 24 of the 133 (18%) had statistically significant decline, and the remaining 73 (55%) had equivocal results.
Perhaps the most important metric is which map patients select for long term use - SOC or IGCIP. Ninety-six of the 133 (72.1%) participants elected to keep IGCIP for long term use despite prior research that shows that there is a bias for CI recipients to favor their original map over a new map. And, for the 28% for elected to keep their SOC map, the process involves no risk - the deactivated electrodes are simply reactivated. Given these exciting prospective findings, the investigators are now proposing a randomized controlled trial (RCT) for newly activated adult CI recipients with both the CI user and testing audiologist blinded as to program (SOC or IGCIP). The investigators hypothesize that CI recipients randomized to IGCIP will have improved hearing performance as assessed by both word and sentence testing.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, care provider, investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Standard of Care | Active comparator | Other: Standard of CareCochlear Implant programming using standard of care |
| Image-Guided Cochlear Implant Programming | Experimental | Other: Image-Guided Cochlear Implant ProgrammingCochlear Implant programming using Image-Guided Cochlear Implant Programming |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- Adults ≥ 18 years of age that have undergone diagnostic testing for sensorineural hearing loss and are candidates for cochlear implantation will be considered eligible for the study
Key exclusion criteria (7 listed)
- Age < 18 years
- Pre-lingual onset of deafness
- Mini-Mental State Exam < 24 (to remove cognitive decline as a confounding variable)
- Congenital inner ear malformation as detected on pre-operative CT scan performed as routine care
- Non-English speaking (because our audiological speech testing battery is validated for English speakers)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Standard of CarePost Cochlear Implant surgery, subject will receive activation/programming of their implant using Standard of Care | Other | Standard of Care |
| Image-Guided Cochlear Implant ProgrammingPost Cochlear Implant surgery, subject will receive activation/programming of their implant using Image-Guided Cochlear Implant Programming | Other | Image-Guided Cochlear Implant Programming |
Primary outcome
AzBio Sentence Scores at +5 Signal to Noise Ratio (SNR)
Time frame: Month 1 post cochlear implant activation
AzBio Sentence Scores at +5 Signal to Noise Ratio (SNR)
Time frame: Month 3 post cochlear implant activation
AzBio Sentence Scores at +5 Signal to Noise Ratio (SNR)
Time frame: Month 6 post cochlear implant activation
Results and safety
The study was withdrawn before enrolling participants, so there are no results.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Jan 2022.
- Individual participant dataSharing planned: No
Related trials for Cochlear Implant
RecruitingObservational study
Retrospective Analysis of Speech Performance Using the HiRes Ultra and HiRes Ultra 3D Cochlear Implant
Cochlear Hearing Loss
RecruitingObservational study
Retrospectively Investigating Longitudinal Outcomes in MED-EL SONATA 2 Cochlear Implant Recipients.
Cochlear Implantation, Sensorineural Hearing Loss
Recruiting
Cochlear Implants and Listening Effort: the Interaction of Cognitive and Sensory Constraints
Cochlear Implant Users
Recruiting
Investigating Auditory Processing in the Users of Auditory Brainstem and Cochlear Implants
Deafness
Not yet recruitingObservational study
Mi2000 TICI Follow-up
Hearing Loss, Binaural, Cochlear Implantation
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Robert F. Labadie, MD, PhD principal investigator
Vanderbilt University Medical Center
Benoit M. Dawant, PhD study chair
Vanderbilt University Medical Center
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Image-Guided Cochlear Implant Programming in people with Cochlear Implant, run by Vanderbilt University Medical Center at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: withdrawn, as of the sponsor's last update on 20 Jan 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was withdrawn before enrolling participants, so there are no results.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
AzBio Sentence Scores at +5 Signal to Noise Ratio (SNR) (time frame: Month 1 post cochlear implant activation). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Jan 2022.