ITMCTR2000003253
Not Yet Recruiting
Phase 1
The clinical effect and biomechanical mechanisms of Peony and licorice decoction fumigation treatment for poststroke strephenopodia: a randomized controlled pilot trial
Dongzhimen Hospital affiliated to Beijing University of Chinese Medicine0 sitesTBD
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Dongzhimen Hospital affiliated to Beijing University of Chinese Medicine
- Status
- Not Yet Recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. confirmed stroke patients with results from computed tomography (CT) or magnetic resonance imaging (MRI);
- •2\. aged between 35 and 75 years, male or female;
- •3\. first episode of stroke or with a history of stroke but with no serious neurofunctional disablility and modified Ranking Scale (mRS) grade \<\= 2;
- •4\. stable condition after stroke and within 6 months of the duration;
- •5\. with strephenopodia and be able to walk at least 6 meters;
- •6\. blood pressure lower than 160/100 mmHG;
- •7\. sufficient cognition to follow commands and Mini\-Mental State Examination (MMSE) score \>\=24;
- •8\. never used fumigation treatment before;
- •9\. the patients or their legal guardian sign an informed consent.
Exclusion Criteria
- •1\. received surgery or thrombolytic therapy;
- •2\. duration of stroke more than 6 months;
- •3\. stroke without strephenopodia or with but could not walk 6 meters;
- •4\. vital signs are not stable or with worsening conditions such like new infarction or bleeding;
- •5\. combined with other cerebral diseases such as subarachnoid hemorrhage, cerebral hemorrhage, brain tumor, brain trauma and so on;
- •6\. combined with lumbar vertebrae disease, knee joint disease, foot disease and other diseases that can affect the patient's walking gait;
- •7\. combined with severe dysfunction of heart, lung, liver, kidney and blood system;
- •8\. combined with moderate to severe cognitive comprehension or visual impairment that can affet rehabilitation treatment or gait examination;
- •9\. pregnant or lactating women;
- •10\. participating in other clinical trials.
Outcomes
Primary Outcomes
Not specified
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