Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04743258
Other study ID # SONAL SURJEET
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2020
Est. completion date October 2022

Study information

Verified date January 2021
Source Postgraduate Institute of Dental Sciences Rohtak
Contact SONAL CHOWDHARY, MDS
Phone 9992025599
Email sonalsingla@rediffmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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 evaluate dental, skeletal & soft tissue changes achieved with maxillary premolar extraction vs full arch distalization. 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 .


Description:

The present study is a prospective, non-pharmacological, single blind, randomized clinical study to evaluate the skeletal, dental and soft tissue changes with distalization of entire maxillary dentition using bilateral maxillary 1st premolar extraction in comparison with zygomatic miniplates in class II division 1 patients. 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 34 subjects selected from the patients attending the regular OPD at the Department of Orthodontics and DentofacialOrthopaedics for orthodontic treatment. 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 TARGET SAMPLE SIZE - A sample size of 15 per group for the present study was calculated to detect a clinical difference of 3.9 mm with effect size 0.86 at 95% power and 5% significance level. To compensate for 10% dropouts the final sample size was calculated to be 17 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. Cephalometric radiographs will be recorded before treatment and after 6 months of application of NiTi closed coil spring for assessment of hard and soft tissue changes. The pretreatment and post 6 months of application of NiTi closed coil spring the cephalometric radiographs will be analyzed. The relevant values will be entered in a predesigned format. (Annexure III, IV). Soft tissue profile changes between pretreatment and post treatment will be assessed on lateral cephalogram and the raters- orthodontist, laypersons,patients,parents and general dentists will assess changes in facial appearance on a visual analog scale with profile photographs and comparison will be done between the two groups. Patient perception will be assessed using questionare rating by patient regarding various parameters at 1week, 2 weeks, 1 month and 6 months after the placement of zygomatic miniplate or extraction Quality of life will also be assessed using questionnaire rating by patient at pre-treatment, mid-treatment and post treatment. Occlusal status changes between pre and post treatment will be assessed using PAR index(peer assessment rating between 2 groups). 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 34
Est. completion date October 2022
Est. primary completion date April 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: 1. Non growing patients 2. Complete bilateral Class II molar relationship at pre-treatment 3. All permanent teeth upto the second molars should be present 4. No or minor crowding in the maxillary arch 5. Horizontal to average growth pattern. Exclusion Criteria: 1. Subjects with a history of fixed orthodontic treatment. 2. Crossbite 3. Vertical growth pattern 4. Any systemic disease affecting bone and general growth 5. Poor oral hygiene 6. Cleft patients 7. Patients who fail to follow up or undergo complete treatment

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
MAXILLARY PREMOLAR EXTRACTION
Patients will undergo bilateral maxillary 1st premolar extraction before bonding followed by leveling & alignment.
DISTALIZATION
Maxillary arch will be distalized with the help Zygomatic miniplates will be placed bilaterally.

Locations

Country Name City State
India Post Graduate Institute of Dental Sciences Rohtak Haryana

Sponsors (1)

Lead Sponsor Collaborator
Postgraduate Institute of Dental Sciences Rohtak

Country where clinical trial is conducted

India, 

Outcome

Type Measure Description Time frame Safety issue
Primary skeletal angular changes SNA angle Pre & Post after space closure in group 1 & achieving Class I molar relation in group 2 28 months
Primary Maxillary dentoalveolar changes maxillary incisor to NA angle Pre & Post after space closure in group 1 & achieving Class I molar relation in group 2 28 months
Primary Soft tissue changes soft tissue profile changes after distalization evaluated on lateral cephalogram and the raters- orthodontist, laypersons,patients,parents and general dentists will assess changes in facial appearance on a visual analog scale with profile photographs 34 months
Primary overjet & overbite measured in mm Pre & Post after space closure in group 1 & achieving Class I molar relation in group 2 28 months
Secondary mandibular plane angle changes in mandibular plane angle after distalization with zygomatic miniplates & comparison with enmasse anterior retraction with mini implants [Time Frame: 28 months]
Secondary airway changes Changes in the upper-airway size will be measured by using lateral cephalometric radiographs taken before and after distalization [Time Frame: 28 months]
See also
  Status Clinical Trial Phase
Completed NCT04619446 - Dentoskeletal Changes Produced by Growth Modification Appliances in Treatment of Skeletal Class II Malocclusion
Active, not recruiting NCT05171738 - Distalization Via Skeletally-anchored Distaljet Appliance With Two Approaches of Micro-osteoperforations N/A
Completed NCT00248014 - Response of Individuals With Class II Malocclusion Phase 2
Completed NCT01853995 - Mechanism of Class II Correction With Fixed Lingual Mandibular Growth Modificator (FLMGM) Phase 2
Completed NCT01853137 - Fixed Lingual Mandibular Growth Modificator N/A
Completed NCT04814173 - The Efficacy of Tow Mechanics for Total-maxillary-arch-distalization N/A
Recruiting NCT03839303 - Comparison Between Mini Implant Supported Appliance and Headgear in Treatment of Maxillary Excess in Growing Patients N/A
Completed NCT04847492 - Evaluation of Upper Anterior Teeth Retraction Rate Assisted by Two Corticotomy Techniques N/A
Recruiting NCT04810286 - Prefabricated Versus 3D-Printing Myofunctional Appliances N/A
Not yet recruiting NCT03764189 - Evaluation of Micro-osteoperforation on Rate of Maxillary En-masse Retraction N/A
Terminated NCT00957489 - A Prospective Randomized Controlled Trial to Evaluate the Effectiveness of the Two Different Appliances in the Treatment of Class II Division 1 Malocclusion N/A
Active, not recruiting NCT04191070 - Distalization Using Infrazygomatic Crest Miniscrews and Zygomatic Miniplates: A Randomized Clinical Trial N/A
Completed NCT05335824 - The Effect of Autologous Platelet Concentrations on Orthodontic Treatment Time N/A
Completed NCT06133361 - The Effect of Platelet-rich Plasma on the Rate and Type of Orthodontic Tooth Movement N/A
Completed NCT05542745 - Measuring Rate of Anteriors Retraction With Two Different Techniques N/A
Completed NCT05040945 - Evaluation of the Levels of Pain and Discomfort Associated With Two Techniques of Corticotomy N/A
Completed NCT05928143 - Patient Outcomes Associated With Two Accelerated Method of Retraction of Upper Front Teeth N/A
Completed NCT04316403 - Laser-assisted Flapless Corticotomy in Accelerating Canine Retraction N/A
Not yet recruiting NCT03635463 - Effect of Modified Twin Block in Skeletal Class II Growing Females With Mandibular Deficiency N/A
Completed NCT03467555 - Evaluation of Distal Movement of Maxillary Dentition With Zygomatic Miniplates Using Cone Beam Computed Tomography N/A