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NCT06024382 Clinical Trial

The Effect of Low-level Laser Therapy on Functional Treatment of Skeletal Class II Patients

Class II Malocclusion Clinical Trial

Official title:
The Effect of Low-level Laser Therapy on Functional Treatment of Skeletal Class II Patients

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06024382
Other study ID # dentist.1995
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 26, 2022
Est. completion date February 28, 2024

Study information
Verified date March 2024
Source Mansoura University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

this is a controlled clinical trial with 2 groups of patients of class II skeletal discrepancy due to mandibular retrusion one group is treated with twin block functional appliance and the other with twin block combined with low level laser therapy ,the study aims to detect the effect of low level laser on the skeletal outcomes , dentoalveolar outcomes, rate of correction and pain during treatment

Recruitment information / eligibility
Status Completed
Enrollment 24
Est. completion date February 28, 2024
Est. primary completion date December 30, 2023
Accepts healthy volunteers No
Gender All
Age group 9 Years to 14 Years
Eligibility Inclusion Criteria: - Age (early permanent dentition) - Cervical maturation stage CS 3-4 - Skeletal class II due to mandibular retrusion. - Overjet more than 4mm. Exclusion Criteria: - Cleft lip or palate. - Systemic diseases. - Previous orthodontic treatment or abnormal habits. - Congenital craniofacial deformity. - poor oral hygiene

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• twin block
2 parallel groups one is treated with twin block and the other is treated with twin block combined with low level laser therapy
• twin block combined with low level laser
2 parallel groups one is treated with twin block and the other is treated with twin block combined with low level laser therapy

Locations
Country Name City State
Egypt Faculty of Dentistry Mansoura Dakahleya

Sponsors (1)
Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary treatment time comparison of treatment between the 2 different groups 8 months
Secondary cephalometric measurements digital tracing of pre and post treatment cephalograms of both groups and comparison of linear and angular measurements 8 months
Secondary study cast analysis cast analysis of both groups measuring arch perimeter , intercanine wisth and intermolar width 8 months
Secondary the short form McGill pain questionnaire comparison of questionnaire results between the 2 groups 1 month
See also
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