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Photobiomodulation Therapy on Nerve Repair Using Red and Infra-red Diode Lasers

Comparison Between Photobiomodulation Therapy on Nerve Repair Using Red and Infra-red Diode Lasers in Maxillofacial Region (A Randomized Clinical Trial)

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07403695
Enrollment
30
Registered
2026-02-11
Start date
2025-03-18
Completion date
2026-01-18
Last updated
2026-02-12

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

Conditions

Nerve Injury

Keywords

laser therapy, photobiomodulation, nerve injury

Brief summary

Peripheral nerve injury is a major concern that drastically affects the patient's quality of life. Nowadays, several treatment options are available, including medical treatments, surgical intervention, and others. However, the trending photobiomodulation effect of laser therapy is attracting many dental professionals due to its promising results on nerve rehabilitation. The study is intended to assess and compare laser photobiomodulation using red and infra-red diode lasers on the repair of nerve injury in the maxillofacial region.

Interventions

DEVICE635 wavelength

635 wavelength laser

DEVICE980 wavelength

980 wavelength laser

Sponsors

mona oraby
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
20 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

1. Patient aged range from 20-50 years old 2. Patient suffering from nerve injury in the maxillofacial region for a period of 6 months or more without improvement.

Exclusion criteria

* 1- Patient had undergone micro-neurosurgery to correct neurosensory deficit.

Design outcomes

Primary

MeasureTime frameDescription
visual analogue scale1,2,4,8,12 weeksfrom 1- 10 1 means no pain 10 means worst pain

Secondary

MeasureTime frameDescription
clinical neurosensory test2,4,8,12 weeksfrom S0 to S4 S0 means worst neurosensory function S4 full recovery for neurosensory function

Countries

Egypt

Contacts

PRINCIPAL_INVESTIGATORMona S Oraby

Alexandria University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026