The purpose of this study is to evaluate the therapeutic effect of acupuncture method of "Xing Nao Kai Qiao" for paralysis as an apoplectic sequela in a multicenter randomized and controlled clinical trial and to compare the efficacy between acupuncture and rehabilitation therapy. In addition, evaluating the trial in the view of medical economics.
This study is a multi-center randomized controlled trial comparing three treatment groups.The trial is completed in the following three hospitals: First Teaching Hospital of Tianjin University of Traditional Chinese Medicine (TCM) of China, Tianjin Hospital of TCM of China, and Qingdao Haici Medical group of Shangdong province of China. The total observation period within this study is 24 weeks for each patient. All patients should remain hemiplegia within 15~90 days after stroke. After randomization the patients will receive 4 sessions of 30 minutes' duration during a period of 4 weeks. The outcome measurement is completed both in the different times as follows: before treatment, after the first treatment, 7, 14, 28days after treatment and follow up at 6 months after treatment. 288 patients were randomised into three groups: acupuncture group, rehabilitation group,and acupuncture plus rehabilitation group.The patients in the three groups are blinded as to which treatment method they received. The central randomization is used in this trial, which is performed by the Drug Clinical Research Center of Shanghai University of TCM of China. This trial is performed according to the principles of the Declaration of Helsinki (Version Edinburgh 2000). And the trial protocol has been approved by local institutional review board and ethics committee.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
288
Xing Nao Kai Qiao Acupuncture
Kinesitherapy
Xing Nao Kai Qiao Acupuncture plus Kinesitherapy
First Teaching Hospital of Tianjin University of Traditional Chinese Medicine (TCM)
Tianjin, Tianjin Municipality, China
RECRUITINGScore of neurological defect
Time frame: before treatment, after the first treatment, 7, 14, 28days after treatment and follow up at 6 months after treatment.
Visualized anologue score
Time frame: before treatment, after the first treatment, 7, 14, 28days after treatment and follow up at 6 months after treatment.
Spasm evaluation
Time frame: before treatment, after the first treatment, 7, 14, 28days after treatment and follow up at 6 months after treatment.
Safety evaluation
Time frame: before treatment, after the first treatment, 7, 14, 28days after treatment and follow up at 6 months after treatment.
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.