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Evaluate the Efficacy of Bu-Yang- Huan-Wu Tang(BYHWT)on Ischemic Stroke

Randomized, Double Blind, Placebo Control Trial to Evaluate the Efficacy of Bu-Yang-Huan-Wu Tang(BYHWT)on Ischemic Stroke

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02150252
Enrollment
120
Registered
2014-05-29
Start date
2014-05-31
Completion date
2016-12-31
Last updated
2014-05-29

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

Conditions

Ischemic Stroke

Keywords

Clinical trial, Ischemic stroke, Bu-Yang-Huan-Wu Tang (BYHWT), Gait parameter, Quality of life

Brief summary

* Clinical trial; Ischemic stroke; Bu-Yang-Huan-Wu Tang (BYHWT); Gait parameter; Quality of life Stroke is the third of ten causing death disease constantly, and it also is third of consuming healthy insurance budget. There is 17,000 peoples disable due to stroke every year in Taiwan. Although ischemic stroke patient may use t-PA intravenously treatment within 3 hrs after stroke onset in modern medicine, and no others method may effect to treat ischemic stroke patients, thus, the study about stroke is an important issue. Bu-Yang- Huan-Wu Tang (BYHWT) has been became a main stream for the treatment of stroke after Qing dynasty Wang Qing-Ren theory that is BYHWT may treat stroke due to pattern of qi stagnation and blood stasis in traditional Chinese medicine. A number of researches report that BYHWT can reduce blood viscosity, anti-inflammation, enhancing neuronal regeneration and angiogenesis, but above-mentioned about BYHWT limit in the level of animal study and the scientific evidence is insufficiency in human trial. Therefore, the purpose of the present study was to investigate the therapeutic effect of BYHWT treating ischemic stroke by using a strict clinical trial. * We designed a randomized, double blind, placebo-controlled study to assess the therapeutic effect of BYHWT treating ischemic stroke. The study expects to finish the assessment of 120 patients with ischemic stroke in three years. The study divided into: 1) control group, receive placebo-BYHWT 3.0 g TID every day for continuously 6 weeks except ordinary medical care; 2) treatment group, the method is identical control group, but receive BYHWY. The main outcome was according to the changes of gait parameter including Speed, Cadence, Strike length, Gait cycle and Double support; and secondary outcome including the changes of Functional independence measurement scores and Barthel index scores, Ten Meters Walk Test, Short Physical Performance Batter, Berg Balance Test and WHO quality of life-brief (Taiwan Brief). * We predict the results of the present can provide scientific evidence to proof BYHWT can improve neurological deficit and also can improve quality of life in patients with ischemic stroke.

Interventions

DRUGBu-Yang-Huan-Wu Tang

control group,Recruited patients should be received the placebo-BYHWT 3.0 g TID every day for continuously 6 weeks except ordinary medical care; 2) treatment group, the method is identical control group

Sponsors

China Medical University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Age ≧40 and ≦75 2. Stroke is first time 3. Between 15 and 90 day after stroke onset 4. NIHSS score between 5 and 20 5. NIHSS: 6th item, motor function (lower extremities) ≦3 6. Walking is at least 10 meters.

Exclusion criteria

1. Intake anticoagulant agent within one week, such as Heparin, warfarin etc. 2. NIHSS: 6th item, motor function (lower extremities) = 0 (lift 30 degree more than 5 second in supine position) 3. Cannot intake food from oral or intake food complete depend on helper 4. Acute stroke onset within 14 days 5. Gait disturbance due to other factor, such as Parkinson disease, spinal injury, knee joint disorders etc. 6. Cerebellar stroke 7. Pregnancy or lactation 8. Over irritability or anxiety results in cannot assessment 9. Severe traumatic injury or head surgery history 10. Stroke due to cerebral venous thrombosis 11. Systemic disease such as uremia, chronic obstructive pulmonary disorders, or heart failure NYHA ≧ (third degree: mild activity induces dyspnea; fourth degree: dyspnea feeling under rest state) 12. Severe psychiatric disorders such as depression, schizophrenia etc.

Design outcomes

Primary

MeasureTime frameDescription
Gait parameter42days and 84daysThe main outcome was according to the changes of gait parameter including Speed, Cadence, Strike length, Gait cycle and Double support.

Secondary

MeasureTime frame
Functional independence measurement scores and Barthel index scores, Ten Meters Walk Test, Short Physical Performance Batter, Berg Balance Test and WHO quality of life-brief (Taiwan Brief).42days and 84days

Countries

Taiwan

Contacts

Primary ContactChing-Liang Hsieh, M.D., Ph.D
clhsieh@mail.cmuh.org.tw+886-4-22053366

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026