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Visualization of the STN and GPi for DBS

NCT05774041 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 80

Last updated 2025-04-25

No results posted yet for this study

Summary

The purpose of the study is to determine if using SIS System for DBS planning results in less distance between the planned target location and the actual implanted lead location than DBS planning without SIS System.

Conditions

  • Deep Brain Stimulation
  • Parkinson Disease

Interventions

DEVICE

SIS System

FDA-cleared software that enhances standard clinical images for the visualization of structures in the basal ganglia area of the brain which are commonly targeted for DBS lead placement.

Sponsors & Collaborators

  • Surgical Information Sciences Inc.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-10-19
Primary Completion
2025-04-07
Completion
2025-04-07
FDA Device
Yes

Countries

  • United States

Study Locations

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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 NCT05774041 on ClinicalTrials.gov