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Prospective Clinical Observational Study on the Real-World Efficacy of Tipei Angong Niuhuang Wan

Prospective Clinical Observational Study on the Real-World Efficacy of Tipei Angong Niuhuang Wan

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2026000033
Enrollment
Unknown
Registered
2026-01-08
Start date
2026-01-07
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Stroke

Interventions

Exposed group:Routine treatment + Tipei Angong niuhuang pill

Sponsors

Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: All patients who were diagnosed and prescribed Tipei Angong Niuhuang Wan by clinicians (investigators) participating in this registry study, as well as those who fully met the diagnostic criteria but did not use Tipei Angong Niuhuang Wan.

Exclusion criteria

Exclusion criteria: (1) Patients with bilateral fixed and dilated pupils and apnea upon admission; (2) Pregnant or lactating women; (3) Patients diagnosed with collapse pattern (Tuo Zheng) in traditional Chinese medicine.

Design outcomes

Primary

MeasureTime frame
Changes in body temperature;Duration of high fever/fever;Glasgow Coma Scale;National Institute of Health stroke scale;Mini-Mental State Examination;Barthel Index;Cranial Imaging Examination;Modified Rankin Scale;Stroke syndrome Factors Diagnostic Scale;Cardiovascular and Cerebrovascular Events;

Secondary

MeasureTime frame
Cost;EQ-5D-3L;Laboratory Parameters;

Countries

China

Contacts

Public ContactLiu Jia

Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medicine Sciences

marie_liujia@163.com18810877011

Outcome results

None listed

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