Minocycline Accelerates Intracerebral Hemorrhage Absorption (MACHA)
Intracerebral Hemorrhage
About this trial
This is an interventional treatment trial for Intracerebral Hemorrhage focused on measuring Minocycline, hematoma absorption
Eligibility Criteria
Inclusion Criteria: 18-80 years old Spontaneous intracerebral hemorrhage by CT scan Intracerebral hematoma volume is less than 16ml No surgical treatment of hematoma evacuation Exclusion Criteria: Allergies to tetracycline antibiotics Pregnancy or suspected pregnancy (pregnancy test will be done on women with fertility potential) Hepatic and/or renal insufficiency Glasgow Coma Scale of 5 or less Secondary cerebral hemorrhage caused by trauma, arteriovenous malformation, aneurysm, tumor or other reasons Thrombocytopenia (platelet count<75000/mm3) or coagulation dysfunction (INR>1.4) Incapable to take care of themselves in past life (score of Rankin scale before stroke>2) Signed DNR (Do Not Resuscitate)
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Minocycline
Control(starch)
This intervention arm will receive oral or intranasal minocycline capsules 100 mg Q12H, first dose 200 mg, start on the fifth day of cerebral hemorrhage, for 14 days
This arm will receive oral or intranasal administration of identically packaged placebo capsules (starch) 100 mg Q12H, first dose 200 mg, start on the fifth day of cerebral hemorrhage, for 14 days