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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00179101
Other study ID # 040251
Secondary ID
Status Completed
Phase N/A
First received September 13, 2005
Last updated August 11, 2006
Start date April 2004
Est. completion date November 2005

Study information

Verified date August 2006
Source Vanderbilt University
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Observational

Clinical Trial Summary

We will evaluate the effect of deep brain stimulation on the depression and quality of life in Parkinson’s disease. We aim to compare depression pre-operatively and post-operatively in Parkinson’s patients with deep brain stimulation to Parkinson’s patients evaluated and approved for deep brain stimulation but who did not complete surgery. We will also compare quality of life measures between patients with and without deep brain stimulation.


Description:

Deep brain stimulation is an approved therapy for Parkinson’s patients, and this procedure is actively performed at Vanderbilt University Hospital. Questions have been raised concerning the effect of deep brain stimulation on the depression commonly seen in Parkinson’s patients. Through this study, we plan to evaluate and compare the incidence and severity of depression in Parkinson’s patients with deep brain stimulation to those who did not complete the surgery. Primary literature has indicated a general increase in quality of life of those patients receiving DBS, but no studies have compared these two specific patient populations.


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date November 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 50 Years to 85 Years
Eligibility Inclusion Criteria:

- Patients diagnosed with idiopathic Parkinson’s disease.

- Patients who have received neuropsychological testing in preparation for possible deep brain stimulation.

- Patients are within the age of 50 and 85.

Exclusion Criteria:

- Parkinson’s patients not approved for deep brain stimulation on the basis of neuropsychological testing.

- Patients who received deep brain stimulation less than a year ago.

- Patients who do not consent to the study procedures.

Study Design

Observational Model: Defined Population, Primary Purpose: Screening, Time Perspective: Longitudinal


Related Conditions & MeSH terms


Intervention

Procedure:
Deep Brain Stimulation


Locations

Country Name City State
United States Vanderbilt University Nashville Tennessee

Sponsors (1)

Lead Sponsor Collaborator
Vanderbilt University

Country where clinical trial is conducted

United States, 

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