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Comparison of the effects of low-power and high-power lasers in the treatment of Bell's palsy

Comparison of the Effectiveness of High-Intensity Laser Therapy (HPLT) and Low-Level Laser Therapy (LLLT) in the Management of Idiopathic facial nerve palsy (Bell’s palsy)

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20260201068723N1
Enrollment
30
Registered
2026-02-16
Start date
2026-02-20
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Bell's palsy. Bell's palsy

Interventions

Intervention 1: Intervention group: 10 patients with Bell's palsy will undergo 10 sessions of low-level laser treatment. Intervention 2: Intervention group2: 10 patients with Bell's palsy will undergo

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 70 years old 2. Diagnosis of acute unilateral Bell's palsy within the past 10 days. The diagnosis must be made clinically and by ruling out other causes. 3. House-Brackmann scale score =3 at baseline 4. Receive standard drug treatment (corticosteroids ± antiviral drugs) 5. Ability and willingness to provide written informed consent 6. Possibility to attend follow-up meetings until the end

Exclusion criteria

Exclusion criteria: 1. Facial palsy with a cause other than Bell's palsy, such as: stroke, tumors (such as acoustic neuroma), Lyme disease, Ramsey-Hunt syndrome, trauma or surgical injury 2. Previous history of Bell's palsy or facial nerve palsy on the same side 3. History of laser sensitivity or conditions that contraindications to laser use, such as: Photosensitive epilepsy, Use of photosensitizing medications 4. Open wound or active infection or skin disease in the treatment area 5. Presence of malignancy in the face or neck area 6. Pregnancy or breastfeeding 7. major chronic neurological diseases such as MS 8. Participation in other concurrent intervention studies 9. Starting physiotherapy or electrical stimulation before entering the study

Design outcomes

Primary

MeasureTime frame
Facial Disability Index (FDI) score. Timepoint: Before starting laser therapy (time zero), immediately after the end of treatment with 10 laser sessions, and one month after the end of treatment. Method of measurement: A short, self-report questionnaire consisting of 10 items or questions.;House-Brackmann system score. Timepoint: Before starting laser therapy (time zero), immediately after the end of treatment with 10 laser sessions, and one month after the end of treatment. Method of measurement: Evaluation of facial nerve function by physician's examination.;Sunnybrook Facial Grading System score. Timepoint: Before starting laser therapy (time zero), immediately after the end of treatment with 10 laser sessions, and one month after the end of treatment. Method of measurement: Evaluation of facial nerve function by physician's examination.;Electrodiagnostic test findings. Timepoint: Before starting laser therapy (time zero), immediately after the end of treatment with 10 laser sessions, and one month after the end of treatment. Method of measurement: Findings from muscle and nerve conduction studies.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadreza Saadati

Shahid Beheshti University of Medical Sciences

Mohammadrezasaadati1373@gmail.com0098212707471

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026