ClinicalTrials.Veeva

Menu

Effectiveness of Four Mini-screws Supported Hyrax for Maxillary Expansion in Early Adulthood

Cairo University (CU) logo

Cairo University (CU)

Status

Active, not recruiting

Conditions

Transverse Maxillary Deficiency

Treatments

Device: Hybrid hyrax

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This study aims to evaluate the Skeletal and Dento-alveolar expansion in adult patents using Four Mini-screws Supported Hyrax in compare with untreated control group.

Full description

Aim of the study: To evaluate the Effectiveness of Four Mini-screws Supported Hyrax for Maxillary Expansion in Early Adulthood

Methodology:

  • Essential record for orthodontic treatment will be taken.
  • impression with bands on upper first molars will be taken.
  • Four eyelets will be soldered to the body of the hyrax appliance (size 10, Dentaurum, Germany).
  • CBCT will be taken while patient wearing 1 mm thickness vacuum on the lower arch to dis-occlude both arches.
  • Delivery, check the retention and fitness of the appliance.
  • The appliance will be cemented using band cement(compomer).
  • Using 3M contra-angle driver, the screws (Tomas screw size 10, Dentaurum, Germany) will be loaded and inserted.
  • Activation of the appliance by opening it two turns immediately, followed by two turns everyday till cross bite correction or appearance of midline diastema.
  • Closure of the device, and leave the appliance in-situ for five months as a retention.
  • Post-expansion CBCT will be taken and continue fixed orthodontic treatment.

Outcome: skeletal and dento-alveolar expansion will be evaluated

Enrollment

24 patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Unilateral or bilateral Dental posterior cross-bite
  • Skeletal Maxillary constriction
  • Male and female patients.
  • Chronological age (18-30 years).
  • Mid-palatal suture maturation (Grade C,D ) according to F Angileri classification
  • Good oral hygiene.
  • No craniofacial anomalies or syndromes

Exclusion criteria

  • Scissor-bite
  • Orthodontically-treated
  • functional cross bite due to premature occlusal contact
  • patients with a syndrome
  • cleft patients
  • Mid-palatal suture maturation(Grade A.B,E) according to F Angileri classification

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

24 participants in 2 patient groups

Hybrid Hyrax
Experimental group
Description:
these patents will be treated using Four mini-screws supported hyrax
Treatment:
Device: Hybrid hyrax
untreated control group
No Intervention group
Description:
Ethically ,these patents will be treated at the end of the study using the same appliance used for the experimental group

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems