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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01505504
Other study ID # MIRTA-2012
Secondary ID
Status Completed
Phase N/A
First received January 4, 2012
Last updated January 5, 2012
Start date January 2004
Est. completion date December 2011

Study information

Verified date January 2012
Source Brugmann University Hospital
Contact n/a
Is FDA regulated No
Health authority Belgium: Federal Agency for Medicinal Products and Health Products
Study type Observational

Clinical Trial Summary

Weight loss is a frequent problem associated with Alzheimers disease (AD). Mirtazapine has weight loss as a frequent side effect.

The aim of this retrospective study is to check whether mirtazapine 30 mg (once daily) can counteract weight loss in patients with AD or mixed dementia (AD + vascular).


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date December 2011
Est. primary completion date November 2011
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- AD or mixed dementia

- documented weight loss

- mirtazapine 30 mg explicitly prescribed against weight loss

Exclusion Criteria:

- no treatment compliance

- other causes of weight loss

- other interventions against weight loss

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective


Intervention

Drug:
mirtazapine
30 mg at bedtime

Locations

Country Name City State
Belgium CHU Brugmann Brussels

Sponsors (1)

Lead Sponsor Collaborator
Brugmann University Hospital

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary body weight 6 months No
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