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Intraoperative EABR for Decision Making

C

Christoph Arnoldner

Status

Enrolling

Conditions

Vestibular Schwannoma
Hearing Loss

Study type

Observational

Funder types

Other

Identifiers

NCT03745560
1111/2017

Details and patient eligibility

About

In this study patients undergoing simultaneous translabyrinthine vestibular schwannoma resection and cochlear implantation are included. The goal of the study is to correlate the eABR results with postoperative hearing results.

Full description

Patients undergoing translabyrinthine vestibular schwannoma resection are included in the study. Preoperatively an eABR is carried out, as well as before and after tumor resection.

Postoperatively patients are fitted with a cochlear implant as routinely carried out. The postoperative hearing results with cochlear implant are correlated to the eABR results. The study is an observational study since eABR measurements are not part of the study. A correlation between eABR results categorized in three groups (good response, weak response, no response) with monosyllable understanding with cochlear implant (measured with Freiburger monosyllables test).

Enrollment

15 estimated patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients between 18 and 99 years undergoing translabyrinthine vestibular schwannoma resection
  • Patients wanted hearing rehabilitation with a cochlear implant

Exclusion criteria

  • patients who do not want to be part of the study

Trial contacts and locations

1

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Central trial contact

Valerie Dahm

Data sourced from clinicaltrials.gov

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