Effect of CO2 Laser on Enamel White Spot Lesion Formation Around Orthodontic Brackets

Damascus University

Status: Completed

Conditions: White Spot Lesion

Treatments: Other: Placebo; Radiation: CO2 laser irradiation

Study type: Interventional

Funder types: Other

Identifiers

NCT03114475

UDDS-Ortho-01-2017

Details and patient eligibility

About

This study aims to evaluate the clinical effect of CO2 laser on enamel resistance to white spot lesions formation around orthodontic brackets.

25 patients needing fixed orthodontic treatment will participate in the study, the CO2 laser will be applied in a split mouth design around orthodontic brackets in two contrast quarters of mouth in every patient and the other quarters will serve as a control. The white spot lesion formation will be monitored around the brackets during the orthodontic treatment after four and twelve weeks of irradiation with laser.

Full description

Prior to enrollment of each subject into the study, they will be examined completely to determine the orthodontic treatment plan. The operator will inform them about the aim of the study and ask them to provide a written informed consent.

Before brackets' bonding (T0) the operator will evaluate with intraoral clinical examination and take intraoral photographs and evaluate with DIAGNOdent. Then after brackets' placement on teeth, the CO2 laser will be applied to the area of enamel about 2 mm of width around orthodontic brackets in a split mouth design. To blind the intervention sides on patients the control sides will receive nontherapeutic light.

Then intraoral photographs will be taken and the teeth will be assessed with DIAGNOdent (T1).

All patients will be trained to brush their teeth with a tooth paste containing 1100 ppm of fluoride twice a day. After 4 weeks of irradiation (T2) the patients will be examined for white spot lesions formation by clinical examination using Geiger index, photographic examination using AutoCAD 2009 evaluating formation and area percentage of white spot lesions, and the degree of demineralization will be assessed with DIAGNOdent. The all exams will also be done after 12 weeks of irradiation (T3).

Enrollment: 25 patients

Sex: All

Ages: 15 to 25 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult patients with permanent occlusion at age 15-25 years.
• No previous orthodontic treatment
• Good oral hygiene
• Need to orthodontic treatment with fixed appliances

Exclusion criteria

• Patients with systemic diseases or syndromes
• Patients with existence of enamel fluorosis
• Patients with existence of amelogenesis imperfecta or hypocalcified enamel
• Patients with existence of restorations or crowns or carious lesions on the labial surfaces of teeth.
• Patients who received fluoride treatment within the last three months prior to being enrolled in the study.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Triple Blind

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25 participants in 2 patient groups, including a placebo group

CO2 Laser Irradiation

Experimental group

Description:

This group of patients will be treated by splitting the dental arches into four quadrants: upper right, upper left, lower right and lower left. Two quadrants will receive the CO2 laser irradiation whereas the remaining two quadrants will receive no treatment (i.e. the placebo light).

Treatment:

Radiation: CO2 laser irradiation

Placebo

Placebo Comparator group

Description:

A placebo light will be used as if the patient is irradiated with the laser beam.

Treatment:

Other: Placebo