Cochlear Implantation Clinical Trial
Official title:
Voice Guard Processing Evaluation in a Cohort of Subjects Implanted With the Neuro Cochlear Implant System
NCT number | NCT03256097 |
Other study ID # | PIC_12 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | July 25, 2018 |
Est. completion date | May 31, 2022 |
Verified date | January 2023 |
Source | Oticon Medical |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The study aims to compare two different cochlear implant sound processing strategies. All the participants will start off with a sound processing strategy called the XDP (extended performance). At the 3 month stage, half of the participants would randomly be selected and offered a sound processing strategy called the Voice Guard. Following that, the sound processing strategies will be altered and evaluated every 3 months at the 6th, 9th and 12th month of cochlear implant use.
Status | Completed |
Enrollment | 21 |
Est. completion date | May 31, 2022 |
Est. primary completion date | May 31, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: - Individuals aged between 18 and 70 years - Individuals with post-lingual hearing loss - Individuals with no language and speech production disorders - Individuals who are native speakers of English - Individuals meeting NICE candidacy criteria for CI surgery - Individuals undergoing primary unilateral cochlear implantation Exclusion Criteria: - Medical conditions contraindicating CI surgery - Individuals with anatomical anomalies of the auditory system - Individuals with additional mental health issues or and/or cognitive impairment |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Queen Elizabeth Hospital, University of Birmingham NHS Hospitals Trust | Birmingham | West Midlands |
United Kingdom | Addenbrooke's Hospital, Cambridge University Hospitals Trust | Cambridge | Cambridgeshire |
Lead Sponsor | Collaborator |
---|---|
Oticon Medical |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Speech perception scores in quite and in noise | Speech perception with each intervention will be measured and a score between 0 to 100% will be obtained | 12 months | |
Secondary | Patient reported outcome measure | Glasgow Hearing aid Benefit profile will be administered to assess patient reported benefit with each intervention | 12 months |
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