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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06300775
Other study ID # 123789
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 1, 2024
Est. completion date June 1, 2025

Study information

Verified date March 2024
Source Cairo University
Contact Sally mosallam, PH degree
Phone 01004288894
Email sally.mosallam@dentistry.cu.edu.eg.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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


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


Recruitment information / eligibility

Status Recruiting
Enrollment 10
Est. completion date June 1, 2025
Est. primary completion date May 1, 2025
Accepts healthy volunteers No
Gender All
Age group 6 Years to 18 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
modified hyrax
Appliance used for rapid maxillary expansion
quad helix
device use for slow maxillary expansion

Locations

Country Name City State
Egypt Cairo univeristry Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Chewing difficulty the outcome will be measured by visual analogue scale one year
See also
  Status Clinical Trial Phase
Completed NCT02574117 - Cone Beam Computed Tomography for Evaluating Corticotomy-assisted Maxillary Expansion N/A