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Treatment of Depression in Parkinson's Disease Trial - Article


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Paroxetine

Paxil; Paxil CR 




Clinical Trial: Treatment of Depression in Parkinson's Disease Trial

Treatment of Depression in Parkinson’s Disease Trial

This study is currently recruiting patients.

Sponsored by: National Institute of Neurological Disorders and Stroke (NINDS)
Information provided by: National Institute of Neurological Disorders and Stroke (NINDS)

Purpose

The goal of this study is to evaluate the effectiveness and safety of two antidepressants--nortriptyline and paroxetine, compared to placebo in patients with Parkinson’s disease and depression.

Condition Treatment or Intervention Phase
Parkinson Disease
Depression
 Drug: nortriptyline
 Drug: paroxetine
Phase II

MedlinePlus related topics:  Depression;   Parkinson's Disease
Genetics Home Reference related topics:  Parkinson disease

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Safety/Efficacy Study

Official Title: Treatment of Depression in Patients with Parkinson’s Disease

Further Study Details: 

Expected Total Enrollment:  75

Study start: June 2003

Depression is the most common neuropsychiatric disorder found in patients with Parkinson's disease (PD). It causes immense personal suffering and is associated with increased disability and caregiver burden.

Despite the adverse consequences of depression in patients with PD, there are virtually no empirical data to guide clinical treatment. This study will begin to answer some questions on the treatment of depression by testing a SSRI (selective serotonin reuptake inhibitor) antidepressant, paroxetine, a tricyclic antidepressant, nortriptyline, and placebo in a placebo-controlled trial.

A total of 75 patients with PD will be randomized to each of the three arms in a balanced design.

Eligibility

Ages Eligible for Study:  35 Years   -   80 Years,  Genders Eligible for Study:  Both

Criteria

INCLUSION:

  • Parkinson's disease without dementia.
  • Depression.
  • Males or females.

Location and Contact Information

Allison Dicke      1-877-795-4673 

New Jersey
      Robert Wood Johnson Medical School, New Brunswick,  New Jersey,  United States; Recruiting
Allison Dicke  877-795-4673 
Matthew Menza, M.D.,  Principal Investigator

Study chairs or principal investigators

Matthew Menza, M.D.,  Principal Investigator,  Robert Wood Johnson Medical School   

More Information

Study ID Numbers:  R01NS43144
Record last reviewed:  October 2004
Last Updated:  October 13, 2004
Record first received:  June 12, 2003
ClinicalTrials.gov Identifier:  NCT00062738
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005

Resources



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November 23, 2009



Page Updated: June 1, 2005
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