Status:

COMPLETED

A Study on Behavioral and Psychological Symptoms of Dementia

Lead Sponsor:

Johnson & Johnson Taiwan Ltd

Conditions:

Dementia

Eligibility:

All Genders

Brief Summary

The purpose of this observational study is to obtain the current status of patients with Behavioral and Psychological Symptoms of Dementia. This study is also expected to further provide insight into ...

Detailed Description

This is an observational, prospective, multi-center study to obtain information about the symptoms and treatment received for patients with behavioral and psychological symptoms of dementia (BPSD). Pa...

Eligibility Criteria

Inclusion

  • Patients with the diagnosis of dementia according to DSM-IV (Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition) criteria
  • Patients meet one of the following types of Dementia: Dementia of the Alzheimer's Type (AD), Vascular Dementia (VaD), Dementia of Lewy Body (DLB), Parkinson's Disease Dementia (PDD)
  • Patients have one or more active symptoms of Behavioral and Psychological Symptoms of Dementia (BPSD) on Neuropsychiatric Inventory (NPI) and have not received treatment with antipsychotics, mood stabilizers, or antidepressants within 1 month prior to study entry
  • Patients are with caregiver(s) who can give appropriate information about the patients and can assist with the assessment during the study
  • Patients (or a legally acceptable representative) have signed the informed consent form

Exclusion

  • Patients with concurrent other primary major psychiatric disorders (such as Schizophrenia or Bipolar disorder)
  • Patients with history of severe allergies or multiple adverse drug reactions
  • Patients with history or current symptoms of tardive dyskinesia
  • Patients with history of neuroleptic malignant syndrome (NMS)
  • Patients who participated in a clinical trial of any investigational drug within 1 month (30 days) prior to study entry

Key Trial Info

Start Date :

September 1 2007

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

September 1 2008

Estimated Enrollment :

359 Patients enrolled

Trial Details

Trial ID

NCT00641459

Start Date

September 1 2007

End Date

September 1 2008

Last Update

May 23 2014

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