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Inappropriate Medications Associated With Anticholinesterase and/or Memantine Treatment in the Elderly

Completed
Conditions
Alzheimer's Disease
Registration Number
NCT00954616
Lead Sponsor
University Hospital, Limoges
Brief Summary

In each of the 7 French areas that should be involved, patients aged 75 years and over from three different sectors will be included: the geriatric consultation unit (60%) and two kinds of nursing homes, private (20%) and state (10%). Outpatients will be included in chronological order; patients in nursing homes will be included at random. The patients and their families will be asked about the treatments received on the day of inclusion. The inclusion period will extend over a year. The investigating practitioners will be asked to fill in a questionnaire reporting the main clinical data, adverse effects occurrence, and information on the treatment given.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
636
Inclusion Criteria
  • Patients aged 75 years and over identified as having Alzheimer disease and who have been treated for more than 3 months with anticholinesterase and/or memantine
Exclusion Criteria
  • Patients with decompensated chronic condition or acute phase disease

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate the prevalence of PIM use in patients aged 75 years and over treated with anticholinesterase and/or memantine2 years
Secondary Outcome Measures
NameTimeMethod
To identify factors associated with PIM use. To study the relationship between PIM exposure and adverse effects occurrence.2 years

Trial Locations

Locations (6)

CHU Rouen

🇫🇷

Rouen, Bois guillaume, France

CHU Bordeaux

🇫🇷

Pessac, Bordeaux, France

CHU Saint Etienne

🇫🇷

Saint Etienne, France

CH Le Mans

🇫🇷

Le Mans, Le Mans Cedex 1, France

CHU Montpellier

🇫🇷

Montpellier, Montpellier Cedex 5, France

APHP Charles Foix

🇫🇷

Ivry sur Seine, Paris, France

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