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Clinical Trials/NCT01861704
NCT01861704CompletedNot Applicable

Post-market Study to Capture Information Regarding Performance of Extended Wear Hearing Aid Lyric2 Compared to Lyric

Phonak AG, Switzerland2 sites in 1 country177 target enrollmentStarted: April 1, 2011Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
177
Locations
2
Primary Endpoint
Immediate Refit Upon Device Removal

Study Overview

Brief Summary

Randomized post market study comparing Lyric to Lyric2 capturing information regarding comparative performance and safety.

Detailed Description

Randomized post market study comparing extended wear hearing aids Lyric to Lyric2 capturing information regarding comparative performance and safety.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 90 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Aged 18-90 years at the time of enrollment in the study
  • Mild to moderately-severe hearing loss bilaterally, or unilaterally if normal hearing in other ear
  • Fluent in English
  • Willingness to comply with all study requirements

Exclusion Criteria

  • Scuba dives or sky dives
  • Underwater swimming or dives into the water
  • Handicaps that would restrict participation in all the evaluations
  • Hearing loss of neural or central origin
  • Unrealistic expectations regarding benefits and limitations inherent in the devices
  • Chemotherapy within the last six months
  • Compromised immune system
  • Radiation to head or neck
  • Perforated tympanic membrane
  • History of cholesteatoma
  • Active outer or middle ear pathology
  • High levels of anticoagulant therapy
  • Insulin-dependent and/or uncontrolled diabetes
  • Contact dermatitis
  • Bleeding disorder
  • Unwillingness or inability to comply with all study requirements

Outcomes

Primary Outcomes

Immediate Refit Upon Device Removal

Time Frame: Following device removal at the same appointment (Up to 24 hours after removal)

Upon device removal, a qualified audiologist examined subjects' ears to evaluate their availability to be immediately refit with another hearing aid device. It is not uncommon for patients being fitted with these types of devices to experience slight irritation on an initial experience with the device. In particular, those being fit with the Lyric or Lyric2.0 for the first time first undergo the device sizing process, which slightly increases stress on the ear.

Secondary Outcomes

  • Device Comfort(During useful lifespan of device)
  • Gain, Speech Understanding and Sound Quality(During useful lifespan of device)

Investigators

Sponsor
Phonak AG, Switzerland
Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (2)

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