U.S. Phase I preliminary results of use of the Otologics MET Fully-Implantable Ossicular Stimulator

Otolaryngol Head Neck Surg. 2007 Aug;137(2):206-12. doi: 10.1016/j.otohns.2007.03.012.

Abstract

Objectives: The safety of the Otologics Fully-Implantable MET Ossicular Stimulator was assessed in adult patients with bilateral moderate to severe sensorineural hearing loss.

Methods: Surgical implantation of the ossicular stimulator was performed. A repeated-measure, within-subjects design assessed safety and aided sound field thresholds and speech performances with the subject's own, appropriately fitted, walk-in hearing aid(s) and the Otologics Fully-Implantable MET Ossicular Stimulator.

Results: Twenty patients were implanted and activated as part of the Phase I clinical trial. Results demonstrated 10-20 dB of functional gain across audiometric frequencies. Pure tone averages and monaural word recognition scores were slightly better for the walk-in-aided condition, while patient benefit scales favored the postoperative implant-aided conditions.

Conclusion/significance: Although monaural word scores and aided thresholds favored the walk-in-aided condition, preliminary results indicate that the Otologics MET Fully-Implantable Ossicular Stimulator is an alternative to currently available hearing aids in patients with sensorineural hearing loss.

Publication types

  • Clinical Trial, Phase I

MeSH terms

  • Adult
  • Aged
  • Audiometry, Pure-Tone
  • Auditory Threshold
  • Bone Conduction
  • Ear Ossicles
  • Ear, Middle / surgery*
  • Electric Stimulation
  • Female
  • Hearing Aids* / adverse effects
  • Hearing Loss, Sensorineural / physiopathology
  • Hearing Loss, Sensorineural / surgery*
  • Humans
  • Male
  • Middle Aged
  • Prostheses and Implants* / adverse effects
  • Speech Perception
  • Treatment Outcome
  • United States