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:
2025-12-25 @ 4:52 AM
Ignite Modification Date:
2025-12-25 @ 4:52 AM
NCT ID:
NCT03320018
Eligibility Criteria:
Inclusion Criteria:
1. Aged 18 years old or over
2. Presenting to/at Stony Brook University Hospital with acute ischemic stroke
3. Baseline (at admission to study) National Institute of Health Stroke Scale (NIHSS) of ≥ 5
4. Administration of study medication possible within 24 hours of last known well
Exclusion Criteria:
1\. Pre-existing neurological disability (historical NIHSS \> 3); unable to live independently 3. Severe stroke or comorbidities likely to result in patient dying within 3 months 4. Acute or chronic renal failure with calculated creatinine clearance \< 30 5. Liver disease leading to \> 3x elevation in liver transaminases or significant loss of synthetic capacity\* 6. Thrombocytopenia (\<100x10\^9platelets / L blood) 7. Pre-existing infectious disease requiring antibiotic therapy that have a negative interaction with minocycline. (Penicillin, amoxicillin, ampicillin, bacampicillin, carbenicillin, cloxacillin, dicloxacillin, methicillin, mezlocillin, nafcillin, oxacillin, piperacillin, ticarcillin) 8. Pregnancy or nursing. Females of reproductive age will be required to use barrier contraception or abstain from sexual intercourse while on study medications, as minocycline may render oral contraceptives less effective.
9\. Known allergy to tetracycline group of drugs 10. Concurrent treatment with retinoids or ergot alkaloids 11. Inability to safely tolerate the fluid load (iv normal saline or po water) associated with study medication\* 12. Treatment with another investigational drug within the last 30 days that may interfere with this study's medications\* 13. Inability to tolerate or comply with study procedures\*
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT03320018
Study Brief:
Protocol Section:
NCT03320018