Last reviewed · How we verify

NCT03256097

Voice Guard Processing Evaluation in a Cohort of Subjects Implanted With the Neuro Cochlear Implant System

Completed NA Last updated 12 January 2023
What this trial tests

NA trial testing XDP sound processing strategy - Period 0 in Cochlear Implantation in 21 participants. Completed in 31 May 2022.

Timeline
25 July 2018
Primary endpoint
31 May 2022
31 May 2022

Quick facts

Lead sponsorOticon Medical
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingsingle
Primary purposetreatment
Enrollment21
Start date25 July 2018
Primary completion31 May 2022
Estimated completion31 May 2022
Sites2 locations across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Oticon Medical

Who can join

Adults 18 to 70, any sex, with Cochlear Implantation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Cochlear Implantation

Currently open trials in the same condition.

Other Oticon Medical trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03256097.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing