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 @ 11:45 PM
Ignite Modification Date:
2025-12-24 @ 11:45 PM
NCT ID:
NCT04819451
Eligibility Criteria:
Inclusion Criteria:
* Patient is between 18 and 80 years of old;
* Patients with ICH rupture into the ventricle in the primary basal ganglia region or non-aneurysmal subarachnoid hemorrhage confirmed by skull imaging examination;
* Patient is admitted to hospital within 72 hours after onset;
* Informed consent of the patients or their family members, and signed informed consent for CSF replacement treatment.
Exclusion Criteria:
* Non-spontaneous intracranial hemorrhage;
* Time from onset to admission is longer than 72 hours;
* The patient who needs surgical treatment;
* Contraindication of lumbar puncture, such as: cerebral hernia, severe intracranial hypertension, puncture site inflammation, blood system diseases, etc.;
* Patient has other serious diseases, such as heart failure, kidney failure, liver failure, etc;
* Patient or his/her relatives refuse to accept the above research plan.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
80 Years
Study:
NCT04819451
Study Brief:
Protocol Section:
NCT04819451