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Clinical observation of Tibetan medicine Zhenlong Xingnaocapsule in the treatment of limb movement disorder in early recovery from ischemic stroke

Clinical observation of Tibetan medicine Zhenlong Xingnaocapsule in the treatment of limb movement disorder in early recovery from ischemic stroke

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2000004162
Enrollment
Unknown
Registered
2020-09-29
Start date
2020-10-10
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

ischemic stroke

Interventions

Sponsors

Dongzhimen Hospital of Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) It meets the diagnostic criteria of cerebral infarction in western medicine and is anterior circulation infarction; (2) Meet the diagnostic criteria of TCM apoplexy - phlegm and blood stasis; (3) Onset 2 weeks to 1 month; (4) Between the ages of 40 and 80, regardless of gender; (5) Motor function rating scale FMA<=95; (6) Those who agree to participate in this clinical trial and sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with brain parasitic diseases, brain trauma, brain tumors, hemorrhagic transformation after cerebral infarction, epilepsy and other diseases; (2) Previous history of cerebrovascular disease, mRS score >=2 points before the onset of this disease; (3) patients with severe liver and kidney diseases or abnormal liver and kidney function examination (ALT and AS>=1.5 ULN, Cr >1 ULN); (4) Patients with other diseases that need to be treated with drugs similar to the experimental drugs; (5) Patients with heart failure, advanced tumors, severe or progressive diseases of blood or other systems; (6) Suspect or have a history of alcohol or drug abuse; (7) Pregnant or lactating women or those who have recently had family planning; (8) Allergic to this drug or to multiple drugs; (9) Patients with severe cognitive decline, complete aphasia or even disturbance of consciousness.

Design outcomes

Primary

MeasureTime frame
FMA score;MRS scale score;

Secondary

MeasureTime frame
HADS score;EQ-5D score;MoCA score;Fugl-meyer sensory Function score;ADL score;SSA score;NIHSS score;Apoplexy syndrome Factor Evaluation Scale;

Countries

China

Contacts

Public ContactZhou Li
Zhouljk7211@163.com+86 13366959763

Outcome results

None listed

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