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 @ 5:05 PM
Ignite Modification Date:
2025-12-24 @ 5:05 PM
NCT ID:
NCT00128050
Eligibility Criteria:
Inclusion Criteria:
* Male or female, aged 18-75 years inclusive
* Intraparenchymal primary supratentorial intracerebral hemorrhage requiring surgical evacuation
* Any Glasgow Coma Score (GCS) score
* Surgery expected to be performed within 24 hours from symptoms onset
Exclusion Criteria:
* Age below 18
* Intraparenchymal hematoma secondary to rupture of cerebral aneurysm or bleeding of arteriovenous (A-V) malformation or cerebral tumors
* Contemporary involvement in another study
* Pregnancy
* Myocardial infarction in the six months preceding enrolment
* Coronary or carotid stents positioned in the six months preceding enrolment
* Solid organ transplant patients (e.g., heart, lung, liver, kidney)
* Pregnancy
* Myocardial infarction in the six months preceding enrolment
* Coronary and carotid stents positioned in the six months preceding enrolment
* Solid organ transplant patients (e.g., heart, lung, liver, kidney)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT00128050
Study Brief:
Protocol Section:
NCT00128050