Influence of Low Level Laser Therapy on the Rate of Orthodontic Tooth Movement and Associated Pain

NCT ID: NCT05120102

Last Updated: 2021-11-22

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 45 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-08-01
• Study Completion Date: 2023-08-30

Brief Summary

This is a single blind randomized controlled trial with split mouth design including 45 patients with extractions of maxillary 1st bicuspids. First leveling and alignment will take place till 17 × 25 Stainless Steel wire pass passively through all the brackets. Canine retraction will be done through elastomeric ligatures maintaining force of 150gm on both sides. One of side of maxillary arch will be irradiated by diode laser (aluminum-gallium-arsenide) of 980nm on cervical, middle, and apical third on buccal and palatal surface of cuspid and the other side will act as placebo. Laser irradiation will be done at baseline and then for 3 more consecutive visits. Measurements will be recorded from maxillary canine hook to maxillary 1st molar hook at 3 weeks interval till complete canine retraction will be achieved. Patients will be given a questionnaires supported numeric scale to record their pain score for a week.

Detailed Description

First ethical approval for the study is going to be taken from the scientific committee and then Institutional Review Board of Dow University of Health Sciences. After getting informed consent from the chosen study participants, banding and bonding of the maxillary arch are going to be done through conventional fixed appliance Edgewise brackets. Initial leveling and alignment are going to be achieved by using nickel titanium and round stainless-steel wires until 0.017x0.025-inch stainless-steel wire passes passively through all fixed appliance. Anchorage is going to be implemented by skeletal anchorage through mini implants and molar stops on 0.017×0.025-inch stainless-steel wire just mesial to upper 1st molar band slot. As this study features a split mouth design so, every study subject will receive Gallium-Aluminum-Arsenic diode laser with a wavelength of 980nm ± 10nm on one maxillary canine and a placebo effect on the other maxillary canine. The side receiving laser irradiation is going to be alternated with every consecutive patient. To prevent from chauffeuring effect, a plastic shield will be used. The patient will be given questionnaire based scale to record pain score for a week.

Distalization of the canines is going to be accomplished by elastomeric chain (Medium span, Ortho Organizer) which can begin instantly after extraction of first premolars. There is no distinction between retraction rate of canines using either elastomeric chain or Nickel Titanium springs.

All study measurements will be taken using 0.01mm with digital Vernier caliper considering hook of maxillary cuspid teeth and hook of maxillary 1st molar teeth as reference points. Measurements will be recorded thrice in a single visit and mean is taken to avoid bias. Readings will be recorded after every three-weeks interval until one of the canines is completely retracted. Arch length will be measured on the cast as inter molar width. Patients will be given a questionnaire supported numeric scale to record their pain score for a week.

Conditions

Orthodontic Appliance Complication

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Experimental side of the arch

The right or left side of the patients maxillary arch selected by randomization

Group Type: EXPERIMENTAL

Diode laser

Intervention Type: DEVICE

K2 diode laser of 980nm wavelength

Placebo side of the arch

The right or left side of the patients maxillary arch selected by randomization

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Diode laser

K2 diode laser of 980nm wavelength

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• age between 15-30 years
• Patients having symmetric extraction of maxillary 1st bicuspids
• All dentitions till 2nd molars should be erupted in the arch

Exclusion Criteria

• Patients with Long term medication or with a history of radiotherapy or chemotherapy.
• Patients with Parafunctional habit.
• Patients with severe tooth displacement (ectopic canine), patients with missing teeth and impacted teeth (except third molars).
• Tooth morphological anomalies especially in the maxillary canines determined clinically or on OrthoPantomoGram/periapical X-rays.
• Patients with any systemic or metabolic disorder or bone pathology.

• Minimum Eligible Age: 15 Years
• Maximum Eligible Age: 30 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Dow University of Health Sciences

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Imtiaz Dr Ahmed, FCPS

Role: STUDY_DIRECTOR

Supervisor

Locations

Dow university of health sciences

Karachi, Sindh, Pakistan

Site Status: RECRUITING

Countries

Pakistan

Central Contacts

Hafiza M Khurshid, MDS

Role: CONTACT

Phone: 03432459580

Email: mammarry21@gmail.com

Facility Contacts

Hafiza M Khurshid, MDS

Role: primary

Other Identifiers

DuhsDikiohs

Identifier Type: -

Identifier Source: org_study_id