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:
2025-12-26 @ 10:58 AM
Ignite Modification Date:
2025-12-26 @ 10:58 AM
NCT ID:
NCT00774306
Eligibility Criteria:
Inclusion Criteria:
* Acute subarachnoid hemorrhage, Hunt-Hess Grades I-IV
* Within 48 hours of admission
Exclusion Criteria:
* Grade V subarachnoid hemorrhage
* Being treated with a lipid-lowering agent
* Contraindication to phenytoin, valproate, or levetiracetam (e.g. history of allergy to one of these agents)
* Contraindication to receiving no antiepileptic drug treatment (e.g. history of pre-existing epilepsy, seizure activity on admission EEG)
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT00774306
Study Brief:
Protocol Section:
NCT00774306