Trials / Completed
CompletedNCT06544603
Laser Acupuncture for Traumatic Facial Paralysis
Effect of Laser Acupuncture for Traumatic Facial Paralysis: A Retrospective Study
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 174 (actual)
- Sponsor
- Beijing Tongren Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
Objective: The objective of this study was to determine whether laser acupuncture therapy could relieve symptoms in patients with traumatic facial paralysis. Methods: This study was retrospective study including 174 patients that undergoing traumatic facial paralysis. All the patients received laser acupuncture (LA). Patients were assigned to the LA 1 month group, LA 3 month group and LA 6 month group, with 58 patients in each group. Clinical outcome measure comprised the House-Brackmann grading system, Facial Clinimetric Evaluation Scale (FaCE), Sunnybrook facial grading scale (SBFG), Facial Disability Index (FDI), electroneuronography (ENoG), electromyography (EMG) and Blink reflex
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Multiwave Locked System (MLS) laser | Laser probe directly contacts with skin of the all the acupoints. The probe was fixed on each point for 1 min. In this study, the laser acupuncture used have wavelength of 808 nm and 905nm, 1.2 W power (808nm is 1 W, 905 nm is 200 mW), continuous mode emission (808 nm) and pulsed mode emission (905 nm) |
Timeline
- Start date
- 2020-01-01
- Primary completion
- 2024-07-10
- Completion
- 2024-07-10
- First posted
- 2024-08-09
- Last updated
- 2024-08-09
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT06544603. Inclusion in this directory is not an endorsement.