NCT02150252

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
120

participants targeted

Target at P50-P75 for phase_2

Timeline
Completed

Started May 2014

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2014

Completed
26 days until next milestone

First Submitted

Initial submission to the registry

May 27, 2014

Completed
2 days until next milestone

First Posted

Study publicly available on registry

May 29, 2014

Completed
2.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2016

Completed
Last Updated

May 29, 2014

Status Verified

May 1, 2014

Enrollment Period

2.6 years

First QC Date

May 27, 2014

Last Update Submit

May 27, 2014

Conditions

Keywords

Clinical trialIschemic strokeBu-Yang-Huan-Wu Tang (BYHWT)Gait parameterQuality of life

Outcome Measures

Primary Outcomes (1)

  • Gait parameter

    The main outcome was according to the changes of gait parameter including Speed, Cadence, Strike length, Gait cycle and Double support.

    42days and 84days

Secondary Outcomes (1)

  • 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

Study Arms (1)

BY HWT,placebo-BY HWT , Gait parameter

EXPERIMENTAL
Drug: Bu-Yang-Huan-Wu Tang

Interventions

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

BY HWT,placebo-BY HWT , Gait parameter

Eligibility Criteria

Age40 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • Intake anticoagulant agent within one week, such as Heparin, warfarin etc.
  • NIHSS: 6th item, motor function (lower extremities) = 0 (lift 30 degree more than 5 second in supine position)
  • Cannot intake food from oral or intake food complete depend on helper
  • Acute stroke onset within 14 days
  • Gait disturbance due to other factor, such as Parkinson disease, spinal injury, knee joint disorders etc.
  • Cerebellar stroke
  • Pregnancy or lactation
  • Over irritability or anxiety results in cannot assessment
  • Severe traumatic injury or head surgery history
  • Stroke due to cerebral venous thrombosis
  • 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)
  • Severe psychiatric disorders such as depression, schizophrenia etc.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

China Medical University Hospital

Taichung, Taiwan, 40447, Taiwan

RECRUITING

MeSH Terms

Conditions

Ischemic Stroke

Interventions

bu-yang-huan-wu-tang

Condition Hierarchy (Ancestors)

StrokeCerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Central Study Contacts

Ching-Liang Hsieh, M.D., Ph.D

CONTACT

Study Design

Study Type
interventional
Phase
phase 2
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 27, 2014

First Posted

May 29, 2014

Study Start

May 1, 2014

Primary Completion

December 1, 2016

Study Completion

December 1, 2016

Last Updated

May 29, 2014

Record last verified: 2014-05

Locations