Crowding, Tooth, Long Face Syndrome, Malocclusion
Conditions
Keywords
orthodontics, vertical dimension, premolars extraction, long face
Brief summary
The aim of the current clinical trial was to evaluate the effects of premolar extractions compared with non-extraction orthodontic treatment on the skeletal vertical dimension of the face. The null-hypothesis is that there is no difference in post-treatment skeletal vertical characteristics of normodivergent and hyperdivergent patients treated orthodontically with first premolar extractions compared with patients treated in non-extraction manner.
Detailed description
The current protocol will be submitted for partial fulfillment of the PhD requirements in Faculty of Dentistry, Cairo University. The trial will be conducted in the outpatient clinic of the Orthodontic Department, Faculty of Dentistry, Cairo University. Primary examination and diagnosis of the patients seeking orthodontic treatment will be performed, to select a sample of the trial. then, final diagnosis and planing of each participant will be performed by a trained orthodontists to be sure that all patients fallen with the inclusion criteria. Interventions will be conducted with the same orthodontist, under supervision of orthodontic professors in the Orthodontic department, Cairo University.
Interventions
orthodontic treatment with teeth extraction
DEVICENon-extraction orthodontic treatment
Non-extraction orthodontic treatment
Sponsors
Cairo University
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Masking description
the outcome assessor will be masked about the group of the participant during the measuring the outcome ..
Intervention model description
-Interventions Intervention Group (I) Extraction treatment group. Bonding all cases will be performed by the principal investigator, then premolars extraction will be done, then installing the 1st alignment wire. Comparator group (C): Non-extraction group. Same orthodontist will bond all the cases and install the 1st alignment wire.
Eligibility
Sex/Gender
ALL
Age
11 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Normodivergent and hyperdivergent patients * Cases with moderate crowding. * Borderline cases which could be treated with extraction or non-extraction strategies
Exclusion criteria
* Hypodivergent patients. * Cases with extremely sever crowding. * Patients with high caries index or periodontal problems. * Patients with systemic diseases, or syndromic conditions.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes in Vertical Dimension (VD) | after 1year. Changes will be measured before the start of trial and at the end of space closing stage, which anticipated to be within 12 months of intervention | Vertical dimension of the face will be assessed by measuring a distances in millimeters between vertical points as ANS-Me (lower facial height), also it will be measured form angles in a degrees as angle SN/MP |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Changes in Overbite | 1 year . Changes will be measured before the start of trial and at the end of space closing stage, which anticipated to be within 12 months of intervention | Distances in millimeters will be measure directly in patient mouth by using caliper it will be measured in millimeters. |
Countries
Egypt
Contacts
Primary ContactHasan A Alrubaie, MSc
Backup ContactAmira A Aboulnaga, PhD ortho
Outcome results
None listed