A Randomized Trial Comparing Two Electroacupuncture Waveforms for Different Severity Groups of Bell Palsy

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Bell palsy (BP) is the most common cause of acute facial palsy, which leads to functional and esthetic disturbances for patients and results in a lowered quality of life. Electroacupuncture (EA) received attention as an alternative and complementary treatment method. The low-frequency continuous wave EA and the intermittent wave EA have been used in the management of BP. The aim of this study is to compare the efficacy and safety of these two electroacupuncture waveforms for different severity groups of BP.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Diagnosed as BP by specialist.

• The score of FNGS 2.0 ≥ 15 at the day 21 since the onset of BP.

• 18 years ≤ age ≤ 65 years.

• Received prednisolone within 72 hours since initial symptoms of BP, the prednisolone dose used was 60 mg per day for 5 days and then reduced by 10 mg per day.

• Signed informed consent and volunteered to participate in this study.

Locations
Other Locations
China
Hangzhou First People' s Hospital, Hangzhou
RECRUITING
Hangzhou
The First Affiliated Hospital of Zhejiang Chinese Medical University
RECRUITING
Hangzhou
The Third Affiliated hospital of Zhejiang Chinese Medical University
RECRUITING
Hangzhou
Contact Information
Primary
Jing Sun, MD, Ph.D
sunjing0268@163.com
86-13429610268
Backup
Zhiyuan Bian
bianbk55@163.com
86-18668128321
Time Frame
Start Date: 2023-11-15
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 120
Treatments
Experimental: Low-frequency continuous wave group
Low-frequency continuous wave EA In each treatment session, the subjects will receive EA treatment. The selected acupoints for needling will be BL2, GB1, GB14, ST2, SI18, ST6, ST4, ST7, SJ17, EX-HN16, EX-HN5, on affected side, and LI4, bilaterally. After the de-qi sensation is achieved, electrical stimulator will be connected to BL2-GB1, and ST4-ST6, and 2Hz continuous wave will be used for 20 min.
Experimental: Intermittent wave group
Intermittent wave EA In each treatment session, the subjects will receive EA treatment. The selected acupoints for needling will be BL2, GB1, GB14, ST2, SI18, ST6, ST4, ST7, SJ17, EX-HN16, EX-HN5, on affected side, and LI4, bilaterally. After the de-qi sensation is achieved, electrical stimulator will be connected to BL2-GB1, and ST4-ST6, and 40Hz intermittent wave will be used for 20 min.
Related Therapeutic Areas
Sponsors
Collaborators: The First Affiliated Hospital of Zhejiang Chinese Medical University, Zhejiang University
Leads: The Third Affiliated hospital of Zhejiang Chinese Medical University

This content was sourced from clinicaltrials.gov