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 @ 9:18 PM
Ignite Modification Date:
2025-12-24 @ 9:18 PM
NCT ID:
NCT03242304
Eligibility Criteria:
Inclusion Criteria:
* Age between 60 and 90 years.
* Agreeing to participate in the study.
* Acute Ischemic Stroke of anterior vascular territory and/or posterior vascular territory whithin 24 hours of onset.
* Nine or more points in the Glasgow Coma Scale.
* Female patients in menopause.
* Patients without cognitive impairment before AIS according to family reference.
* Acceptance of the next of kin proxy in case the participant has sensory impairment.
Exclusion Criteria:
* Age \<60 or \> 90 years.
* Hemorrhagic Stroke.
* Transient ischemic attack (TIA).
* Acute Ischemic Stroke after 24 hours of onset.
* Hormonal replacement therapy.
* Immunosuppressive therapy in the last month before AIS (example corticosteroids).
* Acute infection (Example, pneumonia, urinary tract infection).
* Diagnosis of oncologic disease in the last month before AIS.
* Diagnosis of endocrinologic disease in the last month before AIS.
* Acute or long-term psychiatric illness.
* No agreement to participate in the study.
* Eight or less points in the Glasgow Coma Scale.
* Female patients with menstrual cycle or in the perimenopause.
* Patients with kidney or hepatic illness.
* Patients with cognitive impairment before AIS.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
60 Years
Maximum Age:
90 Years
Study:
NCT03242304
Study Brief:
Protocol Section:
NCT03242304