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prospective Evaluation of the in - vitro Platelet function as well as the concentration of platelets in the cerebrospinal fluid in patients with aneurysmal SAH

Recruiting
Conditions
I60
Subarachnoid haemorrhage
Registration Number
DRKS00009244
Lead Sponsor
eurochirurgische Klinik, UKSH Kiel
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
350
Inclusion Criteria

Age > 18 years; aneurysmal SAH;
informed consent (if patient is not conscious - a custodian will be determined by the responsible legal institution); primary SAH; Aneurysm closure < 48 hours after rupture

Exclusion Criteria

non - aneurysmal SAH; fisher °I ( no SAH visible on primary cranial CT Scan); pregnancy; life expectancy < 1 year

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
DCI („delayed cerebral ischemia) in the first 6 weeks
Secondary Outcome Measures
NameTimeMethod
outcome after 6 weeks: degree of disability after a stroke, using mRS (Modified Rankin Scale)
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