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Clinical effect of Naoxueshu oral liquid on patients with spontaneous cerebral hemorrhage: a single-center, open, non-randomized controlled study

Clinical effect of Naoxueshu oral liquid on patients with spontaneous cerebral hemorrhage: a single-center, open, non-randomized controlled study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051271
Enrollment
Unknown
Registered
2021-09-17
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-08-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

spontaneous intracerebral hemorrhage

Interventions

Group A1:Without surgical treatment and without taking Naoxueshu oral liquid
Group A2:After surgical treatment but did not take Naoxueshu oral liquid.
Group B1:Take Naoxueshu oral liquid without surgical treatment
Group B2:After surgical intervention and taking Naoxueshu oral liquid

Sponsors

North China University of Science and Technology Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients who were confirmed by magnetic resonance imaging ((MRI)) and computerized tomography ((CT)) and met the criteria for the diagnosis and treatment of SICH approved in the AHA/ASA guidelines were selected; 2. The amount of supratentorial bleeding <= 30ml, the displacement of midline does not exceed 5mm, and the amount of subependental bleeding <= 10ml; 3. Aged 18 to 80 years; 4. Select SICH patients within one week of onset; 5. The NIHSS score is between 2 and 20; 6. Obtain the informed consent of the patient.

Exclusion criteria

Exclusion criteria: 1. Patients with severe dysarthria, hearing impairment, cognitive impairment and other reasons cannot cooperate with the scale assessment; 2. Patients with loss of consciousness and disturbance of consciousness; 3. Due to the insufficiency of important organs such as the heart, liver and kidney, the researchers believe that they are not suitable to participate in this researcher; 4. Patients with severe mental illness.

Design outcomes

Primary

MeasureTime frame
Volume of hematomas;Severity of brain edema;Serious adverse events;

Secondary

MeasureTime frame
Liver function;Renal function;Coagulation function;Neural function evaluation;Blood routine;

Countries

China

Contacts

Public ContactChen Tong

North China University of Science and Technology Affiliated Hospital

ct.1973@163.com+86 15032915731

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026