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Product Surveillance Registry; Ear, Nose &Amp; Throat - NIM Vital Cohort

NCT06637995 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 205

Last updated 2025-09-24

No results posted yet for this study

Summary

The purpose of this study is to confirm clinical safety and performance of Medtronic's NIM Vital™ System and accessories when used as intended in a real-world setting.

Conditions

  • Intracranial Surgery
  • Extracranial Surgery
  • Intratemporal Surgery
  • Extratemporal Surgery
  • Neck Surgery
  • Spine Surgery
  • Thoracic Surgery
  • Upper Extremity Surgery
  • Lower Extremity Surgery

Interventions

DEVICE

Intraoperative Nerve Monitoring

Observational data collection from Locating, Stimulating, and Monitoring target nerves during a surgical procedure (clinician standard of care)

Sponsors & Collaborators

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-01-27
Primary Completion
2025-07-03
Completion
2025-07-03

Countries

  • Germany

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06637995 on ClinicalTrials.gov