Cerebral hemorrhage
Conditions
Interventions
ICH+NBO:NBO
ICH:Oxygen
Sponsors
Affiliated Hospital of Jiujiang University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. 18-80 years old, male or female; 2. The included event was spontaneous parenchymal hemorrhage, and no progressive aggravation was observed within 24 hours of onset, including supratentorial and subatentorial; 3. Agree to participate in the clinical trial and sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Simple ventricular hemorrhage, subarachnoid hemorrhage, and brainstem hemorrhage; 2. Massive intracerebral hemorrhage and cerebral hernia requiring craniotomy; 3. The patient has uncontrollable hypertension (systolic blood pressure is greater than 180mmhg or diastolic blood pressure is greater than 110mmhg after drug treatment; 4. Known history of severe chronic obstructive pulmonary disease or asthma (forced expiratory vital capacity less than 1.0L or oxygen dependent); 5. New York Heart Association grade III heart failure; 6. Coma (GCS = 2; 8. Participating in other clinical research.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| National Institute of Health stroke scale;Modified Rankin Scale;IL-18;Caspase-1; | — |
Secondary
| Measure | Time frame |
|---|---|
| Randomized 14-day CTP brain perfusion improvement; | — |
Countries
China
Contacts
Public ContactBao Bing
Affiliated Hospital of Jiujiang University
Outcome results
None listed