Root Resorption in Class II Div 1 Malocclusion in Upper 1st Premolar Extraction vs Distalization

A Comparative Evaluation of Root Resorption Using CBCT, Patients and Orthodontists Perceptions in Class II Division I Malocclusion With Bilateral Extraction of Maxillary First Premolar vs Full Arch Distalization : A Randomized Clinical Trial

Rationale: Class II Division 1 malocclusion is characterized by upper anterior teeth protrusion resulting in upper lip protrusion and convex facial profile, which are considered esthetically unfavorable. Treatment of class II malocclusion due to maxillary protrusion can be done with bilateral maxillary first premolar extraction followed by en-masse retraction of upper anterior teeth using mini implants placed between maxillary 2nd premolar & 1st molar.

Treatment of class II malocclusion due to maxillary protrusion without premolar extraction frequently requires distalization of maxillary molars into Class I molar relation by means of extra-oral or intraoral forces. Absolute skeletal anchorage, available 24 hours a day is an alternative method for molar distalization. Zygomatic miniplates fixed at a distance from the root apices, allows distalization of entire dentition as there is no interference between the fixation device and roots of the teeth.

Aims and Objectives: To quantify root resorption seen with bilateral extraction of maxillary first premolars (followed by en - masse retraction of anterior teeth) vs full arch distalization with zygomatic miniplates in Class II Division I malocclusion.

Method of study: Patients will be allocated randomly to 2 groups-G1 and G2. Patients in G1 will undergo bilateral maxillary 1st premolar extraction before bonding followed by leveling & alignment. Maxillary arch will be stabilized with the help of 0.019"×0.025" stainless steel wire. Hooks will be soldered on archwire used for stabilizing dentition. Mini implants will be placed under local anaesthesia between maxillary 2nd premolar & 1st molar. Ni-Ti closed coil spring will be used to apply a force for en masse retraction of maxillary anterior teeth .

In G2, treatment will be initiated by bonding 0.022" slot MBT preadjusted edgewise appliance. Maxillary arch will be stabilized with the help of 0.019"×0.025" stainless steel wire. Zygomatic miniplates will be placed bilaterally. Hooks will be soldered on archwire used for stabilizing dentition. Ni-Ti closed coil spring will be used to apply a force .

Study Overview

• Status: Recruiting
• Conditions: Class II Div 1 Malocclusion
• Intervention / Treatment: Procedure: maxillary Ist premolar extraction; Procedure: SURGICAL

Detailed Description

The present study is a prospective, non-pharmacological, single blind, randomized clinical study to quantify root resorption seen with bilateral extraction of maxillary first premolars (followed by en - masse retraction of anterior teeth) vs full arch distalization with zygomatic miniplates in Class II Division I malocclusion. The present study will be conducted in the Department of Orthodontics and Dentofacial Orthopaedics, in conjunction with the Department of Oral and Maxillofacial Surgery, P.G.I.D.S., Pt. B.D.Sharma University of Health Sciences, Rohtak. The study will be carried out after the institutional approval obtained from the ethical committee.

SOURCE OF DATA The study sample consists of 30 subjects selected from the patients attending the regular OPD at the Department of Orthodontics and Dentofacial Orthopaedics for orthodontic treatment.

Patients who fail to follow up or undergo complete treatment TARGET SAMPLE SIZEA sample size of 14 per group for the present study was calculated to detect a clinical difference of 0.25 with a pooled standard deviation of 0.2 (effect size 1.56) at 90% power and 95% confidence interval.

To compensate for 10% dropouts the final sample size was calculated to be 15 per group.

INFORMED CONSENT OF THE PATIENT AND AGREEMENT TO BE RANDOMIZED A valid, written informed consent of the patient or parent/ guardian and an agreement to be randomized will be obtained from the patient before registering the patient in this clinical study. Patient will be informed about all the theoretical risks and benefits of the intervention under test (Annexure I). The patient will be given 72 hours to discuss the study with his/her family and take the decision regarding participation in the study.

RANDOMIZATION & ALLOCATION CONCEALMENT Randomization will be done by a person not involved in the trial using computer generated randomization list. The study subjects will be blinded regarding intervention group.

INTERVENTION AND DESIGN OF STUDY The main intervention in this prospective clinical study is the extraction of bilateral maxillary first premolars before initial leveling and alignment with retraction of anterior teeth using mini implants in first group (G1) and is the placement of zygomatic miniplates after initial leveling and alignment of maxillary dental arch in second group(G2) . The study consists of 2 groups with equal allocation of subjects in each group:- Group 1 (G1):- In this group, bilateral maxillary 1st premolars will be extracted followed by Levelling & alignment with 0.022" MBT preadjusted edgewise appliance. Maxillary arch will be stabilized with the help of 0.019" × 0.025" stainless steel wire. Placement of Mini implants bilaterally between maxillary 2nd premolar & 1st molar under LA. Hooks will be soldered on archwire used for stabilizing dentition. Ni-Ti closed coil spring will be used to apply force . Regular follow up of the patient will be done and records including cephalograms and study models will be taken post 6 months of application of NiTi closed coil spring Group 2 (G2):- In this group treatment will be initiated with 0.022" MBT preadjusted edgewise appliance. Maxillary arch will be stabilized with the help of 0.019" × 0.025" stainless steel wire. After that, bilateral Maxillary third molar will be extracted, if present followed by placement of zygomatic miniplates bilaterally under LA.Hooks will be soldered on archwire used for stabilizing dentition. Ni-Ti closed coil spring will be used to apply force . Regular follow up of the patient will be done and records including cephalograms and study models will be taken post 6 months of application of NiTi closed coil spring DATA COLLECTION The investigator will record the patient's name, address and contact number and other relevant case history records (Annexure II) will be taken. CBCTwill be recorded before treatment and after completion of tratment to evaluate root resorprion. The relevant values will be entered in a predesigned format. (Annexure III, IV).

STATISTICAL ANALYSIS The data will be entered into Microsoft Excel and analyzed using SPSS 21(Statistical Package For Social Sciences) package for relevant statistical comparison. Results will be presented in the form of tables and graphs.

Descriptive statistics and inferential statistics will be used. Data will be checked for normality. In all the analysis, the level of significance will be set a 5 percent.

• Study Type: Interventional
• Enrollment (Anticipated): 30
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: DR. SONAL CHOWDHARY, MDS; Phone Number: 9992025599; Email: sonalsingla@rediffmail.com
• Study Contact Backup: Name: DR.VIRENDER SINGH, MDS

Study Locations

• India
  • Haryana
    • Rohtak, Haryana, India, 124001
      • Recruiting
      • Sonal Chowdhary
      • Contact: Sonal chowdhary, MDS; Phone Number: 9992025599; Email: sonalsingla@rediffmail.com
      • Principal Investigator: SONAL CHOWDHARY, MDS

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Non growing patients
• Complete bilateral Class II molar relationship at pre-treatment
• All permanent teeth upto the second molars should be present
• No or minor crowding in the maxillary arch
• Horizontal to average growth pattern.

Exclusion Criteria:

• Subjects with a history of fixed orthodontic treatment.
• Crossbite
• Vertical growth pattern
• Any systemic disease affecting bone and general growth
• Poor oral hygiene
• Cleft patients
• Patients who fail to follow up or undergo complete treatment

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: EXTRACTION OF MAXILLARY IST PREMOLARS; Experimental: EXTRACTION treatment of class II div 1 malocclusion with bilateral maxillary premolar extraction	Procedure: maxillary Ist premolar extraction; Procedure/Surgery: Patients will undergo bilateral maxillary 1st premolars extraction before bonding followed by leveling & alignment.
Experimental: DISTALIZATION; Experimental: DISTALIZATION treatment of class II div 1 malocclusion with distalization using zygomatic miniplates	Procedure: SURGICAL; Surgery:After leveling and alignment,placement of zygomatic miniplates in bilaterally

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
1.To quantify root resorption seen with bilateral extraction of maxillary first premolars (followed by en-masse retraction of anterior teeth) vs maxillary full arch distalization using zygomatic miniplates in Class II division 1 malocclusion.	pre treatment and post treatment cbct has been assessed to measure the root resorption of maxillary teeth in millimetres 2. To compare both patients' and orthodontist's perceptions of treatment being done in both the groups.	34 MONTHS

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
patient and orthodontist perception	patient and orthodontist perception in both the groups has been evaluated using Visual Analogue Scale	34 months

Collaborators and Investigators

• Sponsor: Postgraduate Institute of Dental Sciences Rohtak

Study record dates

Study Major Dates

• Study Start (Actual): June 15, 2021
• Primary Completion (Anticipated): November 30, 2022
• Study Completion (Anticipated): December 15, 2022

Study Registration Dates

• First Submitted: November 12, 2022
• First Submitted That Met QC Criteria: November 28, 2022
• First Posted (Estimate): December 6, 2022

Study Record Updates

• Last Update Posted (Estimate): December 6, 2022
• Last Update Submitted That Met QC Criteria: November 28, 2022
• Last Verified: November 1, 2022

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Stomatognathic Diseases; Tooth Diseases; Tooth Resorption; Malocclusion; Root Resorption; Malocclusion, Angle Class II
• Other Study ID Numbers: SONAL RAVEENA

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: Yes
• IPD Plan Description: STUDY PROTOCOL
• IPD Sharing Supporting Information Type: Study Protocol

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No