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 @ 2:34 AM
Ignite Modification Date:
2025-12-25 @ 2:34 AM
NCT ID:
NCT05630534
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)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
80 Years
Study:
NCT05630534
Study Brief:
Protocol Section:
NCT05630534