Clinical Trials Directory

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

TypeNameDescription
DEVICEMultiwave Locked System (MLS) laserLaser 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.