TCTR20230405002
Not yet recruiting
Phase 1
Efficacy and safety of electroacupuncture combined with external application of traditional Chinese medicine in the treatment of Bell 's palsy: a randomized controlled study
Hongmei Ma0 sites164 target enrollmentApril 5, 2023
ConditionsThis study aims to evaluate the clinical efficacy of electroacupuncture combined with external application of traditional Chinese medicine (EATCM) in the treatment of Bell 's palsy (BP), and to explore the ideal treatment for idiopathic facial paralysis and provide a basis for clinical rehabilitation.electroacupunctureexternal application of traditional Chinese medicineBell 's paralysisrandomized controlled study
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- This study aims to evaluate the clinical efficacy of electroacupuncture combined with external application of traditional Chinese medicine (EATCM) in the treatment of Bell '
- Sponsor
- Hongmei Ma
- Enrollment
- 164
- Status
- Not yet recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •(1\) Patients with diagnosis of idiopathic facial neuritis (Bell 's palsy), and the diagnostic criteria referring to the Chinese Guidelines for the diagnosis and treatment of idiopathic facial paralysis
- •(2\) Patients aged be equal or greater than 18 years and less than or equal to 70 years
- •(3\) First attack, unilateral facial paralysis
- •(4\) Onset time within 1 month, the grading of House\-Brackmann scale be equal or greater than grade 3
- •(5\) Patients voluntarily joined this study and signed an informed consent form.
Exclusion Criteria
- •(1\)Central facial paralysis, or facial paralysis caused by Lyme disease, encephalitis, tumor and other reasons;
- •(2\)Patients with severe mental illness or unconsciousness that could not cooperate with the treatment;
- •(3\)There were wounds and scars at the treatment site affecting the treatment;
- •(4\)Allergic to the study drug;
- •(5\) Patients participated in or were participating in other experimental studies in the past 1 month.
Outcomes
Primary Outcomes
Not specified
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