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The efficacy and safety of Naoxueshu oral liq in the treatment of chronic subdural hematoma: a prospective open label trial

The efficacy and safety of Chinese herbal medicine (Naoxueshu oral liquid) in the treatment of chronic subdural hematoma: a prospective open label trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090565
Enrollment
Unknown
Registered
2024-10-08
Start date
2021-01-28
Completion date
Unknown
Last updated
2024-10-15

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

Conditions

chronic subdural hematoma

Interventions

Naoxue Shu oral liquid treatment group:Naoxueshu Oral Liquid taken orally, 10ml each time, 3 times a day, for 90 days

Sponsors

Beijing Tiantan Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 89 Years

Inclusion criteria

Inclusion criteria: ? Age =18 and <89 years old; ? Diagnosedwith CSDH using head computed tomography (CT) scans ormagnetic resonance imaging; ? Markwalder grade scale = 2 and Glasgow scores = 13; ? Neurosurgeon made a judgment that cerebral hernia would not occur and surgical operation might not be performed in a short time, or patient refused surgical treatment; ? No signs of cerebral hernia; ? Patients provided written informed consent.

Exclusion criteria

Exclusion criteria: ?Known hypersensitivity to any ingredients of Naoxueshu oral liquid; ?Removal surgery for tracranial hematoma has been planned within 15 days; ?Hematoma caused by tumors, blood and other known comorbidities; ?Patients had been on oral Steroids for >1 week; ?Patients had been on oral Statin for >1 week; ?Patients with abnormal platelet count or coagulation function; ?Chronic liver disease, liver and kidney dysfunction, elevated ALT ( >3 times the upper limit of normal value), elevated blood creatinine (> 2 times the upper limit of normal value); ?Patients with heart and lung dysfunction; ?Patients with a tendency towards severe bleeding or re bleeding; ?Patients may receive unconventional anticoagulant treatment with ordinary heparin or low molecular weight heparin during the trial process; ?Patients with an expected lifespan of less than 1 month or those who are unable to complete the study for other reasons; ?Pregnant or breastfeeding; ?Participation in clinical studies of other investigational drugs within 30 days; ?Unable to understand and/or comply with research procedures and/or follow-up due to mental illness, cognitive or emotional disorders; ?For any reason, the researchers believe that the case is not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Hematoma volume;

Secondary

MeasureTime frame
Markwalder grading scale;Barthel Index;recurrence;

Countries

China

Contacts

Public ContactFan Yongping

Beijing Tiantan Hospital Affiliated to Capital Medical University

yongpingf@hotmail.com+86 10 5997 6662

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026