Neurophysiological Intraoperative or Epilepsy Monitoring

Patients Operated on at the Neurosurgery Department Clinical Trial

— nphysdocu  

Official title:

Retrospective Data Analysis of Neurophysiological Data for Intraoperative or Epilepsy Monitoring

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT01630785
• Other study ID #: nphysdocu
• Status: Enrolling by invitation
• Start date: January 2012
• Est. completion date: December 2025

Study information

• Verified date: November 2023
• Source: University of Zurich
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

The investigators record the outcome of patients whose surgery involved intraoperative neurophysiological monitoring

• Trial with surgical intervention

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 5000
• Est. completion date: December 2025
• Est. primary completion date: December 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 0 Years to 100 Years

Eligibility

Inclusion criteria: Patients whose surgery involved intraoperative neurophysiological monitoring

Related Conditions & MeSH terms

• Epilepsy
• Patients Operated on at the Neurosurgery Department

Intervention

Device:
• Intraoperative Neurophysiological Monitoring IONM
Intraoperative Neurophysiological Monitoring IONM device. Manufacturer: Inomed, Emmendingen, Germany

Locations

Country	Name	City	State
Switzerland	University Hospital Zurich, Neurosurgery	Zurich	ZH

Sponsors (1)

Lead Sponsor	Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	oncological outcome	overall survival, progression free survival	5 years
Primary	neurological outcome	validated scales like Karnofsky or NIHSS	1 year
Primary	seizure outcome	ILAE classification of epilepsy surgery outcome	1 year