SO03-01 - EVALUATION OF THE EFFECT OF N-3 SUPPLEMENTATION ON FUNCTIONAL IMPROVEMENT IN POSTSTROKE PATIENTS - SO3-01
- Conditions
- Post ischemic stroke
- Registration Number
- EUCTR2009-014730-22-IT
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Authorised-recruitment may be ongoing or finished
- Sex
- All
- Target Recruitment
- Not specified
Principal inclusion criteria are: Patients of all ages; Patients of both sexes Patients malnourished and well-nourished Patients with previous ischemic stroke
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
Principal exclusion criteria are: presence of other neurological diseases malignancies or progressive and degenerative diseases; severe liver disease; severe renal insufficiency. patients with score > 20 at mini mental test examination (for the exclusion of dementia) patients treated with antidepressants for less than a week
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method