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Evaluation of the efficacy of transcranial repetitive stimulation combined with electroacupuncture in the treatment of facial paralysis.

Evaluation of the efficacy of transcranial repetitive stimulation combined with electroacupuncture in the treatment of facial paralysis.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000762
Enrollment
Unknown
Registered
2024-12-01
Start date
2024-01-01
Completion date
Unknown
Last updated
2024-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Facial paralysis

Interventions

control group:Conventional acupuncture combined with electroacupuncture.
Transcranial Repetitive Needle Stimulation Group:Transcranial repetitive needle acupuncture combined with electroacupuncture.

Sponsors

Xiamen University Affiliated Xiang'an Hospital Traditional Chinese Medicine Department
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Meet the diagnostic criteria for Bell's palsy; 2. First occurrence unilateral onset; 3. Onset within =3 days; 4. Patients with H-B facial nerve function grade II to IV (mild to moderate) at the initial consultation; 5. No other related treatments received prior to consultation; 6. Aged between 18 and 80 mentally normal and capable of daily living; 7. Able to accept and cooperate with transcranial repetitive stimulation acupuncture treatment and voluntarily sign the informed consent form; Only those who meet the above criteria can be included in this study.

Exclusion criteria

Exclusion criteria: 1. Facial paralysis secondary to other diseases such as viral infections trauma tumors otitis media etc.; 2. Other types of facial paralysis that do not meet the inclusion criteria such as Hunter's facial paralysis etc.; 3. Accompanied by systemic diseases such as heart and kidney dysfunction hypertension diabetes etc.; 4. Pregnant women; 5. Individuals with severe infections in the facial area; 6. Those participating in other clinical trials and unable to comply with treatment plan arrangements;

Design outcomes

Primary

MeasureTime frame
House-Brackmann facial nerve paralysis grading;

Secondary

MeasureTime frame
The difference in facial temperature of the subjects before and after treatment.;

Countries

China

Contacts

Public ContactZhang Chunfang

Xiang'an Hospital Xiamen University

cfzhang@xah.xmu.edu.cn13904809839

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026