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

Primary Purpose

Ischemic Stroke

Status
Unknown status
Phase
Phase 2
Locations
Taiwan
Study Type
Interventional
Intervention
Bu-Yang-Huan-Wu Tang
Sponsored by
China Medical University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ischemic Stroke focused on measuring Clinical trial, Ischemic stroke, Bu-Yang-Huan-Wu Tang (BYHWT), Gait parameter, Quality of life

Eligibility Criteria

40 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • China Medical University HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

BY HWT,placebo-BY HWT , Gait parameter

Arm Description

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

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).

Full Information

First Posted
May 27, 2014
Last Updated
May 27, 2014
Sponsor
China Medical University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02150252
Brief Title
Evaluate the Efficacy of Bu-Yang- Huan-Wu Tang(BYHWT)on Ischemic Stroke
Official Title
Randomized, Double Blind, Placebo Control Trial to Evaluate the Efficacy of Bu-Yang-Huan-Wu Tang(BYHWT)on Ischemic Stroke
Study Type
Interventional

2. Study Status

Record Verification Date
May 2014
Overall Recruitment Status
Unknown status
Study Start Date
May 2014 (undefined)
Primary Completion Date
December 2016 (Anticipated)
Study Completion Date
December 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
China Medical University Hospital

4. Oversight

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemic Stroke
Keywords
Clinical trial, Ischemic stroke, Bu-Yang-Huan-Wu Tang (BYHWT), Gait parameter, Quality of life

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
BY HWT,placebo-BY HWT , Gait parameter
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Bu-Yang-Huan-Wu Tang
Intervention Description
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
Primary Outcome Measure Information:
Title
Gait parameter
Description
The main outcome was according to the changes of gait parameter including Speed, Cadence, Strike length, Gait cycle and Double support.
Time Frame
42days and 84days
Secondary Outcome Measure Information:
Title
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).
Time Frame
42days and 84days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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. Exclusion Criteria: 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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ching-Liang Hsieh, M.D., Ph.D
Phone
+886-4-22053366
Ext
3500
Email
clhsieh@mail.cmuh.org.tw
Facility Information:
Facility Name
China Medical University Hospital
City
Taichung
ZIP/Postal Code
40447
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ching-Liang Hsieh, M.D., Ph.D
Phone
+886-4-22053366
Ext
3500
Email
clhsieh@mail.cmuh.org.tw

12. IPD Sharing Statement

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

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