Dutch Intracerebral Hemorrhage Surgery Trial pilot study
- Conditions
- Intracerebral hemorrhage (intracerebrale bloeding)Minimally invasive surgery (minimaal invasieve chirurgie)
- Registration Number
- NL-OMON22738
- Lead Sponsor
- Radboud University Medical Center(on behalf of the CONTRAST consortium)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 400
Inclusion Criteria
1. Age ≥ 18
2. NIHSS ≥ 2 (Table 2)
Exclusion Criteria
1. Pre-stroke disability, which interferes with the assessment of functional outcome at 90 days, i.e. mRS > 2 (Table 1)
2. Causative vascular lesion (e.g. aneurysm, AVM, DAVF, CVST) on CTA or other known underlying cause (e.g. tumor, cavernoma)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method