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 @ 10:45 PM
Ignite Modification Date:
2025-12-24 @ 10:45 PM
NCT ID:
NCT00088335
Eligibility Criteria:
INCLUSION CRITERIA
Patients between ages 18 to 80 years who are able to give informed consent.
Before any study related procedure is undertaken, the subject or his representative must sign a consent form.
In those individuals with dementia, a legal guardian will need to sign the consent form prior to any procedure.
EXCLUSION CRITERIA
Medical disorders such as lupus, diabetes, serious heart and kidney disease, thyroid dysfunction and any chronic medical illness with the exception of hypertension and hypercholesterolemia.
Patients with any history of bleeding diatheses or abnormal platelets or PT/PTT. Patients using anticoagulants and other drugs which can alter PT/PTT.
Patients with evidence of elevated intracranial pressure based on the imaging studies.
Pregnant women
Children
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT00088335
Study Brief:
Protocol Section:
NCT00088335