Phase I Deep Brain Stimulation (DBS) vs. Best Medical Therapy (BMT) Trial

US Department of Veterans Affairs (VA)

Status and phase

Completed

Phase 3

Conditions

Parkinson's Disease

Treatments

Device: Bilateral Deep Brain Stimulation

Other: best medical therapy

Study type

Interventional

Funder types

Other U.S. Federal agency

NIH

Identifiers

NCT00056563

468 Phase I

Details and patient eligibility

About

The goals of this study are to determine if simultaneous bilateral subthalamic nucleus stimulation or simultaneous bilateral globus pallidus stimulation is more effective in reducing symptoms of Parkinson's disease, and if deep brain stimulation or best medical therapy is more effective in improving Parkinson's disease symptoms

Full description

Deep Brain Stimulation (DBS) is a promising therapy for Parkinson's disease (PD). Whether DBS is superior to comprehensive best medical therapy or whether some patients or symptoms respond better to DBS in one area of the brain or the other is currently not known. The goals of this project are to compare the effectiveness of DBS and comprehensive medical therapy as treatments for PD, and to compare bilateral DBS at 2 areas of the brain--the subthalamic nucleus (STN) and the globus pallidus (Gpi)--to determine the most effective brain site for surgical intervention In this prospective, randomized, multi-center trial, 316 patients will be enrolled at 13 centers over four and a half years. Patients will initially be randomized to immediate surgery (DBS) or to 6 months of "best medical therapy." BMT patients will then proceed into the surgical phase of the trial. The DBS site (STN or GPi) will be assigned on a random basis at the time the patient enters the surgical phase of the trial. Patients will be followed for two years post surgery (24-30 months). Effective 08/05/05, randomization to the BMT arm has been discontinued since the study has sufficient information to compare the outcomes of DBS and BMT patients at 6 months. The findings will be critically important in establishing the optimal surgical treatment of the disabling symptoms of PD.

Enrollment

255 patients

Sex

All

Ages

22+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

idiopathic Parkinson's disease,
Hoehn and Yahr stage 2 or worse "off" medications,
L-dopa responsive but with persistent disabling symptoms (i.e., refractory to "best medical treatment" with motor fluctuations, dyskinesias),
on stable medical therapy for at least one month prior to enrollment,
age > 21,
available and willing to be followed-up according to study protocol, and
no intracranial abnormalities that would contraindicate surgery (based on pre-operative magnetic resonance imaging of the brain).

Exclusion criteria

"Parkinson's plus" syndromes,
medical contraindications to surgery or stimulation,
active alcohol or drug abuse,
score on minimental status exam 24 or lower, or other neuropsychological dysfunction (e.g., dementia) that would contraindicate surgery,
concurrent participation in another research protocol.