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Intraoperative Investigation of a Directional Lead and Local Field Potentials for the Optimization of Stimulation Efficacy

NCT03630302 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 10

Last updated 2021-05-28

Study results available
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Summary

The current study aims to explore the functional use of LFPs recorded intraoperatively for the optimization of a directional DBS lead programming

Aim-1: To determine whether intraoperative LFPs recorded from the segmented DBS electrode can predict the optimal stimulation parameters.

Aim-2: Compare the therapeutic window for stimulation delivered through directional and conventional leads and determine if the spatiospectral LFP patterns correlate with the presence of stimulation side effects.

Conditions

  • Parkinson

Interventions

DEVICE

DBS

Deep Brain Stimulation

Sponsors & Collaborators

  • Baylor College of Medicine

    collaborator OTHER

  • University of Houston

    collaborator OTHER

  • Abbott Medical Devices

    lead INDUSTRY

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-07-12
Primary Completion
2019-12-31
Completion
2020-01-31
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 NCT03630302 on ClinicalTrials.gov