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Clinical Trials/NCT03638310
NCT03638310
Completed
Not Applicable

Assessment of Visual Sensitivity, Psychiatric Profile and Quality of Life Following Vestibular Schwannoma Surgery in Patients Prehabituated by Chemical Vestibular Ablation

Charles University, Czech Republic1 site in 1 country37 target enrollmentJanuary 1, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Vestibular Schwannoma
Sponsor
Charles University, Czech Republic
Enrollment
37
Locations
1
Primary Endpoint
change of optokinetic nystagmus measurement
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The aim of this study is to assess effect of psychiatric profile on visual sensitivity and overall health status in patients who underwent surgery for vestibular schwannoma and were prehabituated by chemical vestibular ablation.

Registry
clinicaltrials.gov
Start Date
January 1, 2016
End Date
June 1, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Charles University, Czech Republic
Responsible Party
Principal Investigator
Principal Investigator

Balatkova Zuzana

Zuzana Balatkova, M.D., Principal Investigator, Department of otorhinolaryngology and head and neck surgery,1st faculty of medicine Charles university and University hospital Motol, Prague, Head: Prof. Jan Plzak, M.D., Ph.D.

Charles University, Czech Republic

Eligibility Criteria

Inclusion Criteria

  • T3, T4 vestibular schwannoma
  • recorded growth of a tumour
  • hearing loss greater than 50% in PTA

Exclusion Criteria

  • T1 vestibular schwannomas
  • no growth progression
  • normal hearing

Outcomes

Primary Outcomes

change of optokinetic nystagmus measurement

Time Frame: change of the gain of optokinetic nystagmus among 3 time points is measured: before intervention, 1 week after intervention, 3 months after intervention

During electronystagmography gain of optokinetic nystagmus is measured before and after the intervention

Study Sites (1)

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