Identification of Clinically Relevant Markers of Deep Brain Stimulation Electrode Impedance

Sponsor
University of Florida (Other)
Overall Status
Completed
CT.gov ID
NCT02794233
Collaborator
(none)
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Study Details

Study Description

Brief Summary

The study will look into the changes of Deep Brain Stimulation (DBS) measured impedances in patients of Parkinson disease (PD) as a function of their functional state (lying, sitting and walking) and dopaminergic medication intake (levodopa or dopamine agonists).

The goal is to use DBS measured impedance as a surrogate of the functional and medication states of PD patients.

Condition or Disease Intervention/Treatment Phase
  • Other: Impedance measurements
N/A

Detailed Description

Subjects will be recruited from the population of patients who are already implanted with DBS for treatment of PD.

At the patient's follow up visit they will be asked to come to the clinic in the "off medication" state. Off medication is defined as at least 8 hours since the last medication dosing. Data will be collected during three phases: "OFF" state, transitioning state, and "ON" state. Subjects will be asked to assume different functional states (lying, sitting or walking) for 1 minute each. During these functional states, multiple measures of impedance will be collected.

  • "OFF" state data collection: The subject will be examined to assess his motor examination score using the UPDRS-III. Measurements of impedance will be collected multiple times in the lying down and sitting up states.

  • Transition state data collection: The subject will be asked to take their dopamine medication. The medication will take approximately 1 hour to take full effect. Measurements of impedance will be collected every 10 minutes during this transition from the "OFF" state to the "ON" state. Patients will be asked to report at what point they felt the "ON: state (they can report the state as "OFF", "unsure", "transition" or "ON").

  • "ON" state data collection: The "ON" state examination will start after 1 hour from medication administration. Subjects will be examined using the UPDRS-III. Measurements of impedance will be collected in the lying down, sitting and walking states.

Summary of the study protocol:

"OFF" state Transition state "ON' state UPDRS-III x x Impedance Lying down x x Sitting up x x x Walking x UPDRS I and II x Hoehn and Yahr x x

Study Design

Study Type:
Interventional
Actual Enrollment :
6 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Identification of Clinically Relevant Markers of Deep Brain Stimulation Electrode Impedance
Study Start Date :
Jul 1, 2016
Actual Primary Completion Date :
Jun 1, 2017
Actual Study Completion Date :
Jun 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: PD patients with implanted DBS

Impedance measurements at different time points.

Other: Impedance measurements
Refer to study description

Outcome Measures

Primary Outcome Measures

  1. Change in impedance value as it relates to the functional state. [1 hour (for both outcomes)]

    Functional state is defined as either: lying, sitting or walking.

  2. Change in impedance value as it relates to the dopaminergic medication state. [1 hour (for both outcomes)]

    Dopaminergic medications are defined as either levodopa containing or dopamine agonist containing medications. The state is defined as the "OFF" state (medication effect is not present) and "ON" state (medication effect noted).

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Idiopathic Parkinson's patients with DBS (unilateral or bilateral)

  • Must be taking dopamine agonist or levodopa regimen

  • Medtronic Neurostimulator Activa SC, PC or PC+S (IPG)

Exclusion Criteria:
  • Hoehn and Yahr (H&Y) 4 and above

  • History of DBS revision or lead replacement surgery

  • Current or prior non-Medtronic Activa SC, PC or PC+S IPG

  • Historical information of more than 1 hour delay to "ON" state as average

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Florida, Center for Movement Disorders and Neurorestoration Gainesville Florida United States 32607

Sponsors and Collaborators

  • University of Florida

Investigators

  • Principal Investigator: Leonardo Brito de Almeida, MD, University of Florida

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University of Florida
ClinicalTrials.gov Identifier:
NCT02794233
Other Study ID Numbers:
  • IRB201600567
First Posted:
Jun 9, 2016
Last Update Posted:
May 15, 2018
Last Verified:
May 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Keywords provided by University of Florida
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 15, 2018