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Evaluation of the Anchorage Loss During En-masse Retraction in Orthodontic Patients With Maxillary Protrusion

Evaluation of the Anchorage Loss During En-masse Retraction in Orthodontic Patients With Maxillary Protrusion Using Friction Versus Frictionless Mechanics: A Randomized Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04902456
Enrollment
30
Registered
2021-05-26
Start date
2020-12-29
Completion date
2022-01-29
Last updated
2021-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bimaxillary Protrusion

Keywords

En-masse Retraction, Friction, Frictionless, CBCT, Anchorage, Anchorage loss, Dental models

Brief summary

There is scarcity in literature regarding the effectiveness of friction and frictionless mechanics during ''En-masse retraction''technique on anchorage loss of posterior segment in orthodontic patients with maxillary protrusion. Moreover there is deficiency in studies measuring the patient pain and satisfaction regarding the different techniques of retraction. The aim of the current study is to evaluate the effects of friction versus frictionless mechanics, implemented during En-masse retraction, on anchorage loss. Additionally, assessment of both techniques regarding their rates, effects on root resorption as well as patient satisfaction.

Detailed description

One of the most common complaints of orthodontic patients is proclination of anterior teeth where there is an increase in facial convexity and as well as incompetent lips. Bimaxillary dentoalveolar protrusion and class II division I cases always have this appearance. Frequently this situation requires extraction of the first premolars followed by fixed orthodontic appliance for space closure and retraction of anterior teeth. Different techniques are used including Two-step retraction where canines are retracted as a first step followed by anterior four incisors as a second step and En-masse retraction where anterior teeth are retracted as one unit. However, the method of En-masse retraction is controversial - whether to use frictionless or friction mechanics.

Interventions

PROCEDUREPower chain and Crimpable hook fro En-masse Retraction

Retraction will start on a 0.017x0.025 stainless steel wire using elastomeric chain ( for applied will be 212 g per side ) extending between the cripmable hooks and the miniscrew

PROCEDURET-loop

closing retraction T-loops will be fabricated using 0.017x0.025 TMA wire. The loop will be positioned halfway the extraction space and the canine.

Sponsors

Future University in Egypt
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Only the outcome assessors will be blind. The patients name will be sealed from pre and post radiographs and study models. Then two assessors will carry out, blindly and independently, the measurements and analysis of the study

Eligibility

Sex/Gender
ALL
Age
14 Years to 24 Years
Healthy volunteers
Yes

Inclusion criteria

1. Orthodontic patients (both genders) 2. Age range (14-24) 3. Patients requiring 1st premolars extraction followed by ''En-masse retraction'' (Bimaxillary Protrusion or Class II division 1 cases). 4. Patients with fully erupted permanent teeth (not necessarily including the 3rd molar). 5. Cases requiring maximum anchorage during anterior segment retraction. 6. Cases with minimal crowding (2-3) mm

Exclusion criteria

1. Patients suffering from any systemic diseases interfering with tooth movement. 2. Patients with extracted or missing permanent teeth. (except for third molars). 3. Patients with badly decayed teeth. 4. Patients with any parafunctional habits (i.e. Bruxism, tongue thrusting, mouth breathing, etc....). 5. Patients with previous orthodontic treatment

Design outcomes

Primary

MeasureTime frameDescription
Anchorage lossfrom pre to post retraction/intervention ( an average of 6-8 months )Digitally scanned dental models taken pre and post completion of retraction will be measured by identifying landmarks and reference lines and planes ( measured in mm )

Secondary

MeasureTime frameDescription
Molar Rotationfrom pre to post retraction/intervention ( an average of 6-8 months )Digitally scanned dental models that are taken before and after retraction will be assess the rotation of the maxillary first permanent molar in relation to a reference line ( measurement of the angles in degrees )
Pain of Interventionfrom pre to post retraction/intervention ( an average of 6-8 months )each patient will fill a questionnaire regarding his treatment experience in a Visual Analog Scale (VAS) scoring from 1-10 by making a handwritten mark on a 10-cm line that represents a continuum between no pain on the left end (0 cm) of the scale and the worst pain on the right end of the scale (10 cm). The question-naire will include several questions related to oral hygiene, pain and discomfort experienced throughout the trial.
Retraction Ratefrom pre to post retraction/intervention ( an average of 6-8 months )The antero-posterior movement of anterior teeth and first molars will be assessed by measuring the digitally scanned dental models taken of the patients monthly ( measured in mm )
Anterior teeth torquefrom pre to post retraction/intervention ( an average of 6-8 months )The principle investigator will examine pre and post Cone Beam CT ( CBCT ) in Relation to lines and reference planes ( measured in degrees )
Anterior teeth tipfrom pre to post retraction/intervention ( an average of 6-8 months )The principle investigator will examine pre and post Cone Beam CT ( CBCT ) in Relation to lines and reference planes ( measured in degrees )
Anterior teeth extrusion/intrusionfrom pre to post retraction/intervention ( an average of 6-8 months )The principle investigator will examine pre and post Cone Beam CT ( CBCT ) in Relation to lines and reference planes ( measured in mm )

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026