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Effect of surgically assisted accelerated tooth movement on En-masse retraction

Phase 1
Completed
Conditions
Healthy subjects undergoing routine orthodontic treatment for esthetic reasons, hence requiring extraction of first premolar and en-masse retraction of maxillary anterior.
Registration Number
CTRI/2019/03/018140
Lead Sponsor
Dr Pranav Bhasin
Brief Summary

This is a radomized clinical trial, to compare the duration of en-masse retraction with micro-osteoperforation. The study consist of 60 subjects. which will be randomly divided into experimental and control group, with 30 subjects in each group. Ten micro-osteoperforations will be performed with the help of lane pilot drill, three distal to canine and 2 mesial to canine, bilaterally, just before retraction. The rate of tooth movement is observed every month and treatment duration will be 7 months/ till the completion of canine retraction.

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Patient with Angle’s Class I malocclusion, Angle’s Class I bimaxillary malocclusion and Class II bimaxillary and Angle’s class II div I malocclusion requiring 1st premolar extraction and anterior en-masse retraction 2.
  • Only those patients were included in which atraumatic 1st premolar extraction was done.
  • The performance of MOPs and canine retraction was done at least 4 months after the extraction procedure to remove the bias due to the RAP induced due to extraction.
  • Canine roots to be in cancellous bone.
  • Patient with good oral hygiene.
Exclusion Criteria
  • Patients on long term use of antibiotics, phenytoin, cyclosporine, anti-inflammatory drugs were discarded 2.
  • Patients on systemic corticosteroids and calcium channel blockers were not included in the study.
  • Patients with history of periodontal therapy 4.
  • Patients with untreated caries, gingivitis and h/o smoking were not included in the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To observe the rate of orthodontic tooth movement with micro-osteoperforationtotal time period - 7 months | patient is recalled every 28 days.
Secondary Outcome Measures
NameTimeMethod
To compare the overall treatment time for en-masse retractiontotal time period - 7 months or till the completion of retraction

Trial Locations

Locations (1)

Subharti Dental college, SVSU, Meerut, UP

🇮🇳

Meerut, UTTAR PRADESH, India

Subharti Dental college, SVSU, Meerut, UP
🇮🇳Meerut, UTTAR PRADESH, India
Dr Pranav Bhasin
Principal investigator
09837175914
pranav.bhasin10@gmail.com

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