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 @ 2:48 PM
Ignite Modification Date:
2025-12-24 @ 2:48 PM
NCT ID:
NCT00364559
Eligibility Criteria:
Inclusion Criteria:
* Men or Women \>16 and \< 80 years with ICH and hospital attention in less 24 hours
* Confirmation by CT scan
* Acceptance by family
Exclusion Criteria:
* History of stroke
* History of neurological disease, head injury o psychiatric disorder with disability
* Glasgow less than 9
* Administration 24 hours before: fibrates, niacin, ciclosporin, azoles, macrolides, inhibitors of protease, nefazodone, verapamil, diltiazem, amiodarone.
* Use before hospital of: mannitol, barbiturates, corticosteroids, calcium antagonists
* Any lesion which needs surgery
* Allergy to drug used
* cerebral death
* Hepatic disease (Child B y C) or myopathy (or) history
* Management in other Hospital
* Pregnancy
* ICH major than 60 ml.
* hypothyroidism
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
16 Years
Maximum Age:
80 Years
Study:
NCT00364559
Study Brief:
Protocol Section:
NCT00364559