ITMCTR2100005122Not yet recruiting未知
Clinical effectiveness study of treating postpartum idiopathic facial paralysis by tonifying qi and blood with acupuncture and moxibustion: a randomized, controlled clinical trial
Shuguang Hospital Affiliated to Shanghai University of traditional Chinese Medicine0 sitesStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional study
Eligibility Criteria
- Sex
- Female
Inclusion Criteria
- •1. Onset within 1 year after delivery;
- •2. Meet the diagnostic criteria for idiopathic facial nerve palsy;
- •3. The course of the disease is within 1-7 days;
- •4. The first onset on the affected side;
- •5. Also see limb fatigue and weakness, pale complexion, dizziness, etc., pale red tongue with thin white fur, and thin pulse, which is a syndrome of qi and blood deficiency;
- •6. Those who voluntarily signed the informed consent form.
Exclusion Criteria
- •1. Secondary peripheral facial paralysis, such as facial paralysis caused by trauma, tumor, cerebrovascular disease, intracranial infection, surgery, etc.;
- •2. Hunter syndrome;
- •3. Diabetes, hypertension, other immune-related diseases;
- •4. Use of drugs or treatments that may cause peripheral neuropathy;
- •5. Those with a history of fainting needles;
- •6. Those who are pregnant.
Investigators
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