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
Name Time Method To observe the rate of orthodontic tooth movement with micro-osteoperforation total time period - 7 months | patient is recalled every 28 days.
- Secondary Outcome Measures
Name Time Method To compare the overall treatment time for en-masse retraction total 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, IndiaDr Pranav BhasinPrincipal investigator09837175914pranav.bhasin10@gmail.com