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Clinical Trials/NCT06300775
NCT06300775
Recruiting
Not Applicable

A Comparative Evaluation of Modified Hyrax Versus Quad Helix in Treatment of Children With Posterior Cross Bite: Randomized Controlled Trial

Cairo University1 site in 1 country10 target enrollmentJune 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Posterior Cross Bite
Sponsor
Cairo University
Enrollment
10
Locations
1
Primary Endpoint
Chewing difficulty
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

This study will be performed to evaluate the treatment of posterior cross-bite with modified hyrax & Quad helix appliances and to compare which one will provide better results in relation to chewing difficulty in children with posterior cross- bite in mixed dentition

Detailed Description

This study will be performed to evaluate the treatment of posterior cross-bite with modified hyrax \& Quad helix appliances and to compare which one will provide better results in relation to chewing difficulty as a primary outcome of this study and also evaluate the increase in the inter maxillary width , sleep apnea and signs \& symptoms of tempro-mandibular joints disorder in children with posterior cross- bite in mixed dentition Cases will be examined within a regular interval up to one year

Registry
clinicaltrials.gov
Start Date
June 1, 2024
End Date
June 1, 2025
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sally Mohamed Mosallam

phd researcher student

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Children with posterior cross-bite in mixed dentition stage.
  • Children with normal and mild growth pattern.
  • Children with completely erupted upper first molars.

Exclusion Criteria

  • Children with advanced periodontal diseases.
  • Children having general diseases, syndromes.
  • Children with previous orthodontic.
  • Children with severe horizontal growth patterns.

Outcomes

Primary Outcomes

Chewing difficulty

Time Frame: one year

the outcome will be measured by visual analogue scale

Study Sites (1)

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