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Clinical Trials/NCT02210988
NCT02210988
Completed
Not Applicable

Evaluating the Therapeutic Effect of Acupuncture on Acute Ischemic Stroke Patients

Cathay General Hospital0 sites38 target enrollmentMay 2011
ConditionsAcute Stroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Stroke
Sponsor
Cathay General Hospital
Enrollment
38
Primary Endpoint
National Institute of Health Stroke Scale
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The investigators design a randomized, single blinded, control study to evaluate the therapeutic effect of acupuncture in acute ischemic stroke patients:

Detailed Description

Acupuncture therapy in traditional Chinese medicine has been verified in many disease by thousands years. Due to the feasible and relatively safe in acupuncture management, now the west countries had been well document about acupuncture in medicine. The acupuncture therapy applied in post stroke functional recovery has been considered as more benefit than physical therapy only to post stroke rehabilitation. However, the effect of combined acupuncture therapy with standard management in acute stroke patient still remains unknown. The aim of this study is to evaluate the therapeutic effect of acupuncture in acute ischemic stroke patients. The prospective study was designed as a randomized, single blinded, control trial. We collected newly onset of acute ischemic stroke patient without underling systemic major illness, and randomized assign the collected patients into two groups as experimental (acupuncture)group and normal control group. The two groups both treat with routine western medicine as standard stroke therapy. The outcome measurement will evaluate by the changes from baseline at one and three months. The assessed scales including NIH stroke scale, the Barthel index, the Functional Independence Measure score, the Fugl-Meyer Assessment, and the Modified Rankin Scale. We compared the all variable measurements to see if any benefit from acupuncture group than the control group.

Registry
clinicaltrials.gov
Start Date
May 2011
End Date
May 2012
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • newly onset of acute ischemic stroke,

Exclusion Criteria

  • without underling systemic major illness

Outcomes

Primary Outcomes

National Institute of Health Stroke Scale

Time Frame: the fourth week

Fugal-Mayer Assessment

Time Frame: The fourth week

Functional Independent Measure

Time Frame: The fourth week

Secondary Outcomes

  • Barthel index(The three month after admission)
  • Modified Rankin Scale(The three after admission)
  • National Institute of Health Stroke Scale(The three months after admission)

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