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Clinical Outcomes of Deep Brain Stimulator (DBS) Electrodes Placed Using Intraoperative Computed Tomography (CT) and Frameless Stereotaxis

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01703598
First Posted: October 10, 2012
Last Update Posted: September 20, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Matthew Brodsky, Oregon Health and Science University
  Purpose
The purpose of this study is to determine whether performing deep brain stimulation surgery for Parkinson's disease using intraoperative imaging and frameless stereotaxis is noninferior to using frame-based stereotaxy and microelectrode recording.

Condition Intervention
Parkinson's Disease Device: Deep Brain Stimulation Procedure: DBS surgery

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Intervention Model Description:
Asleep Deep Brain Stimulation
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Clinical Outcomes of Deep Brain Stimulator Electrodes Placed Using Intraoperative Computed Tomography and Frameless Stereotaxis Versus Microelectrode Recording and Frame-based Stereotaxis

Resource links provided by NLM:


Further study details as provided by Matthew Brodsky, Oregon Health and Science University:

Primary Outcome Measures:
  • Change in motor UPDRS in OFF Levodopa state [ Time Frame: Baseline and 6 months ]

Secondary Outcome Measures:
  • Change in PDQ-39 [ Time Frame: Baseline and 6 months ]
  • Change in ON time without dyskinesia- [ Time Frame: Baseline and 6 months ]
    based on motor diary


Enrollment: 32
Study Start Date: September 2011
Study Completion Date: March 2017
Primary Completion Date: March 2017 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: DBS surgery
Single arm
Device: Deep Brain Stimulation
Placement of Deep Brain Stimulation electrodes
Procedure: DBS surgery
Placement of DBS electrodes

  Hide Detailed Description

Detailed Description:

Background: Frame-based stereotaxis and microelectrode recording (MER) with mapping of target structures has been the gold standard for deep brain stimulator (DBS) implantation. Though supported by historical considerations, no Class I or II evidence exists that MER adds significant value to the DBS implant procedure. With the advent of advanced magnetic resonance imaging (MRI) and computed tomography (CT) imaging, particularly intra-operative imaging, the argument for the continued use of MER during DBS implantation has been substantially weakened. One rationale for pursuing CT-guided intraoperative imaging is due to presumed increase in patient comfort with this method. DBS implantation with MER requires that the patient remain awake during the entire procedure. , MER with frame-based stereotaxis requires the patient to keep their head in a fixed position for a prolonged period of time during which time they remain awake, causing significant patient discomfort. Furthermore, Parkinson's disease patients must withhold their PD meds for a minimum of 12 hours prior to the procedure adding a sometimes significant degree of discomfort and anxiety to the procedure.

Objective: The goal of this study is to compare the clinical outcomes of DBS electrodes placed using intraoperative CT and frameless stereotaxis with those placed using MER and frame-based stereotaxis.

Design: The proposed study will be a prospective non-interventional data collection study.

Setting and Subjects: Subjects for this study will be idiopathic Parkinson's disease patients identified from the Oregon Health & Science University movement disorder clinic as candidates for deep brain stimulation therapy. Enrollment will continue until fifty subjects have been implanted with electrodes using frameless stereotaxis and intraoperative CT. Data regarding quality of life, motor control, and amount of time during the day without levodopa side effects will be collected pre-operatively and post-operatively. This data will be compared to historical controls who have been implanted with DBS electrodes using MER and frame-based stereotaxis. All surgical procedures will involve only Federal Drug Administration (FDA) approved stereotactic equipment, used in the manner for which they have been approved. All clinic procedures are standard of care for movement disorders patients in the deep brain stimulation program.

Intervention: This study will be a non-interventional data collection study.

Measurements: Data regarding patient age, diagnosis, intracranial target, complications, Unified Parkinson's Disease Rating Scale UPDRS Parts 3 (motor examination) and 4 (drug side effects), Parkinson's Disease Quality of life PDQ-39, 3 day motor diary, 3 month falls diary, neuropsychiatric evaluation and days in hospital following surgery will be collected.

Analysis: The patients will be examined prior to DBS placement both on and off dopaminergic medications. They will then be examined 3 months and 6 months following DBS placement both on and off drug with stimulator on after programming parameters have been optimized. The following measures will be performed:

  • Change in UPDRS Parts 3 and 4
  • Change in PDQ-39
  • Change in amount of time patient is experiencing Parkinson's disease symptoms and/or side effects of treatment.
  • Change in number of falls
  • Change in neuropsychiatric evaluation, including:
  • Beck Depression Inventory-II (BDI-II)
  • Mattis Dementia Rating Scale-Second Edition (DRS-2)
  • Repeatable Battery for the Assessment of Neuropsychological Status (RBANS)
  • Symptom Checklist-90-Revised (SCL-90-R)
  • Wechsler Abbreviated Scale of Intelligence (WASI) We will also compare the number of days spent in hospital following surgery. Adverse events related to the surgery will be captured.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Idiopathic Parkinson's disease patients identified by OHSU movement disorders neurologists as deep brain stimulation surgical candidates

Exclusion Criteria:

  • Subjects who have already undergone implantation of DBS electrodes 2.Age < - - 18 years
  • Surgical target site other than subthalamic nucleus or globus pallidus pars interna
  • Subjects who choose to undergo MER and frame-based stereotaxis for the placement of electrodes.
  • Patients who will receive follow up neurology care and DBS programming at centers other than OHSU.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01703598


Locations
United States, Oregon
Oregon Health & Science University
Portland, Oregon, United States, 97239
Sponsors and Collaborators
Oregon Health and Science University
  More Information

Responsible Party: Matthew Brodsky, Principal Investigator, Oregon Health and Science University
ClinicalTrials.gov Identifier: NCT01703598     History of Changes
Other Study ID Numbers: IRB00007508
First Submitted: September 9, 2011
First Posted: October 10, 2012
Last Update Posted: September 20, 2017
Last Verified: September 2017

Keywords provided by Matthew Brodsky, Oregon Health and Science University:
Parkinson's disease
Deep Brain Stimulation

Additional relevant MeSH terms:
Parkinson Disease
Parkinsonian Disorders
Basal Ganglia Diseases
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Movement Disorders
Neurodegenerative Diseases