Reversal of Anaesthesia with Diode Laser

NCT06841120 | Completed

• 1 other identifier: RecepTayyipErdoganUniversity
• Study Type: interventional
• Target: 40
• Locations: 1 country
• Sites: 1

Brief Summary

Background: After local anesthesia, which is frequently used in pediatric dentistry, long-term soft tissue numbness can cause various problems. The aim of this study was to evaluate the effectiveness of PBMT in reversing soft tissue anaesthesia in children following local anaesthesia administration. Methods: In a split-mouth randomized study, 40 children aged 4 to 9 years, eligible to receive local infiltration injection on both maxillary (n=20) and mandibular (n=20) right and left sides, will included. Maxillary and mandibular quadrants will be randomly assigned to laser or sham laser groups. Normality will assessed using the Kolmogorov-Smirnov test. Categorical variables between laser and control groups will compared using the McNemar paired sample test. Significance will be set at p\<0.05.

Conditions

Photobiomodulation Therapy

Keywords

photobiomodulation therapy; diode laser; dental local anaesthesia; child

Outcome Measures

Primary Outcomes (1)

• Anesthesia reversal time

  Until the first reversal of anesthesia, a palpation technique will be used to record every 10 minutes. With this technique, the presence of a sense of touch and tingling will be questioned. In order to obtain an objective answer, the child will be asked whether he/she knows what a tingling sensation is based on his/her previous experiences and will be told what and how this sensation is.

  up to 30 minutes after procedure

Study Arms (2)

Actual laser application

EXPERIMENTAL

Device: Actual laser application

Sham laser was applied symbolically

SHAM COMPARATOR

Device: Sham laser application

Interventions

Actual laser application DEVICE

At approximately 45 minutes into the treatment session, subjects in the laser group received irradiation from a 4 W power, 810 nm diode laser (Fox; ARC Laser, GmbH, Nürnberg, Germany). The laser was operated in continuous mode, delivering 12-second shots per point using a therapy head with a point size of 0.38 cm². Each point received 6.3 J/cm² of laser energy, resulting in a total energy density of 37.8 J/cm² across 6 points.

Actual laser application

Sham laser application DEVICE

Sham laser was applied symbolically as a diffused closed laser (targeted beam) at the same distance and simultaneously. Evaluations after laser irradiation were conducted by a responsible specialist physician who was not involved in performing the treatment procedures.

Sham laser was applied symbolically

Eligibility Criteria

• Age: 4 Years - 9 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Child (0-17)

You may qualify if:

• \- Children whose parents signed the written informed consent form and who themselves gave assent,
• Children with a Frankl behaviour rating scale score of 3 or 4,
• Children aged between 4 and 9 years old who can understand soft tissue sensation and respond to it,
• Children requiring treatment with local infiltration anaesthesia for multiple teeth in both the mandible and maxilla,
• Children with no history of allergy to materials used for anaesthesia or sulphite,
• Children who have not taken any analgesic medication at least 24 hours before treatment,
• Children without any systemic conditions that would interfere with dental treatment under local anaesthesia.

You may not qualify if:

• Occurrence of an error during anaesthesia injection resulting in insufficient anaesthesia for treatment,
• Inability of the patient to provide clear assessments of response to soft tissue anaesthesia,
• Presence of systemic conditions that would prevent anaesthesia administration or dental treatment,
• Children requiring urgent dental treatment priority such as acute painful teeth.

Sponsors & Collaborators

• Recep Tayyip Erdogan University: lead

Study Sites (1)

Recep Tayyip Erdoğan University, Faculty of Dentistry

Rize, Rize Province, 53100, Turkey (Türkiye)

Location

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Associate Professor

Study Record Dates

• First Submitted: January 21, 2025
• First Posted: February 24, 2025
• Study Start: January 18, 2023
• Primary Completion: January 18, 2024
• Study Completion: April 30, 2024
• Last Updated: February 24, 2025

Record last verified: 2025-01

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)