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Clinical Trials/EUCTR2006-000287-84-NO
EUCTR2006-000287-84-NO
Active, not recruiting
Not Applicable

Seponering av antipsykotika og antidepressiva hos demente pasienter med APSD i sykehjem - en åpen studie.

Sykehuset Innlandet HF0 sites24 target enrollmentMay 15, 2006
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ConditionsThe included patients are all elderly people with dementia of Alzheimer or vascular type. Their dementia is moderate or severe and they all have Behavioral or Psychological Symptomes (BPSD).MedDRA version: 8.1Level: LLTClassification code 10057678Term: Vascular dementia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
The included patients are all elderly people with dementia of Alzheimer or vascular type. Their dementia is moderate or severe and they all have Behavioral or Psychological Symptomes (BPSD).
Sponsor
Sykehuset Innlandet HF
Enrollment
24
Status
Active, not recruiting
Last Updated
14 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 15, 2006
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •1\. Dementia of Alzheimer or vascular type.
  • •3\. Regulary intake of antipsychotics or antidepressivas daily for three months or more.
  • •4\. Living in Nursing homes for the last three months.
  • •Are the trial subjects under 18? no
  • •Number of subjects for this age range:
  • •F.1\.2 Adults (18\-64 years) yes
  • •F.1\.2\.1 Number of subjects for this age range
  • •F.1\.3 Elderly (\>\=65 years) yes
  • •F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • •1\. Other kind of dementia.
  • •2\. Schizofrenia, depression or another psychiatric disease.
  • •3\. Expected life\-duration less than three months.
  • •4\. Terminal illness.
  • •5\. Acute infection, uncontrolled Diabetes Mellitus or another somatic disease wich may interfere with the dementia and its symptoms.

Outcomes

Primary Outcomes

Not specified

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