Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 2:25 PM
Ignite Modification Date:
2025-12-24 @ 2:25 PM
NCT ID:
NCT01971359
Eligibility Criteria:
Inclusion Criteria:
1\. Inclusion Criteria:
* Consecutive patients aged at 18-80 presenting with an acute symptomatic supratertorial primary ICH diagnosed by CT
* Symptom onset to surgery \<24 hours (target \<8 hours)
* Glascow Coma Score \> 9
* Hematoma Volume, between 10ml and 50ml.
* Minimal or no ventricular extension (corresponding to 50% or less of each ventricle)
* NIHSS of \>4 or deterioration determined by a neurologist.
Exclusion Criteria:
* Suspected secondary ICH
* Infratentorial ICH
* Isolated IVH
* Uncorrected coagulopathy
* Significant premorbid disability (mRS \>1)
* Hydrocephalus
* Contraindication to safe surgical procedure as per neurosurgeon (justification for exclusion on this basis will be recorded)
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
80 Years
Study:
NCT01971359
Study Brief:
Protocol Section:
NCT01971359