Effect of laser diode on the repair of inferior alveolar sensory nerve damage

The comparison of 940nm and 810nm diode laser type effects on the repair of inferior alveolar sensory nerve damage

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190520043644N1

Enrollment

Registered

2019-12-15

Start date

2019-05-27

Completion date

Unknown

Last updated

2019-12-17

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

Conditions

Inferior alveolar sensory nerve damage. Other complications of anesthesia

Interventions

Intervention 1: Intervention group: Under the 810 nm diode laser beam 810nm Laser: Diode laser with GaAlAc medium (Gallium Aluminum Arsenide) with 810nm wavelength manuf

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: With sensory and neuropathic disturbances Sensory nerve damage due to dental treatments Less than 6 months of injury Treated with laser Systemic diseases

Exclusion criteria

Exclusion criteria: Sensory nerve damage is due to trauma Already exposed to laser radiation History of drug addiction Smoking

Design outcomes

Primary

Measure	Time frame
The number of people with a fatigue rating above 3. Timepoint: After the sessions 1, 3, 7 and 12 treatment. Method of measurement: Numerical Scale.;The number of people who tested the clinical neurosensory test. Timepoint: After the sessions 1, 3, 7 and 12 treatment. Method of measurement: Brush Stroke test with the criterion for detecting one of two horizontal and vertical movements, Two Point Discrimination test with a minimum recording distance of less than 10 mm, Thermal Discrimination test with a heat and cold detection criterion, and a Pin Prick Nociception test with a metric for registering more hits. From 30%.	—

Measure

Time frame

The number of people with a fatigue rating above 3. Timepoint: After the sessions 1, 3, 7 and 12 treatment. Method of measurement: Numerical Scale.;The number of people who tested the clinical neurosensory test. Timepoint: After the sessions 1, 3, 7 and 12 treatment. Method of measurement: Brush Stroke test with the criterion for detecting one of two horizontal and vertical movements, Two Point Discrimination test with a minimum recording distance of less than 10 mm, Thermal Discrimination test with a heat and cold detection criterion, and a Pin Prick Nociception test with a metric for registering more hits. From 30%.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactHooman Ebrahimi

Islamic Azad University

hooman.ebrahimi@yahoo.com+98 21 2256 4571

Outcome results

None listed

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