Impact of CD177 on extent of and recovery from disability after ischemic stroke
Recruiting
- Conditions
- I63Cerebral infarction
- Registration Number
- DRKS00030825
- Lead Sponsor
- niversitätsklinikum Essen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 800
Inclusion Criteria
adult patients with first-ever acute (up to 48 hours after symptom onset) ischemic stroke
Exclusion Criteria
previous strokes, subacute or chronic strokes (>48 hours after symptom onset), hemorrhagic strokes, no consent
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method IHSS, Barthel-Index, mRS in the acute phase (24-36 hours after hospital admission), subacute phase (72-96 hours) and chronic phase (3 months) stratified by CD177 status
- Secondary Outcome Measures
Name Time Method Cognition (MoCA), depressive symptoms (PSD questionnaire by Nolte 2006), quality of life (SF12) stratified by CD177 status