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Fu's Subcutaneous Needling Versus Filiform Needling for chronic Bell's Palsy : a protocol for a pilot randomized controlled trial

Phase 1
Conditions
Chronic Bell's Palsy
Registration Number
ITMCTR2200006373
Lead Sponsor
The Second Affiliated Hospital of Guangzhou University of Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

(1) Meet the diagnostic criteria for Bells palsy according to Chiese Society of Neurology.
(2) Have had a course of disease of a minimum one month to maximum six months.
(3) Be aged 18-70 years (either sex).
(4) Be absent of facial spasm symptoms.
(5) Voluntarily accept the study protocol and provide written consent.

Exclusion Criteria

(1) Are proved to have either an uncontrollable or a diagnosed medical conditions that may impact or disrupt treatment, this includes but is not limited to severe liver, kidney, heart, brain disease. uncontrollable or untreated hypertension (if systolic blood pressure > 160 mmHg and/or diastolic blood pressure > 100 mmHg), uncontrollable or untreated diabetes and hyperthyroidism.
(2) Have allergies to needles and metals.
(3) Show bleeding tendencies such as leukemia and thrombocytopenia.
(4) Show severe or extensive infection and rupture of facial skin tissue.
(5) Refuse to receive FSN or filiform needling therapy.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sunnybrook facial grading system;
Secondary Outcome Measures
NameTimeMethod
House-Brackmann facial nerve grading system;
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