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Clinical Trials/NCT04940351
NCT04940351UnknownNot Applicable

Comparative Evaluation of the Effectiveness of Piezocision and Micro-osteoperforation in Alleviating Mandibular Anterior Crowding: A Randomized Clinical Trial

Postgraduate Institute of Dental Sciences Rohtak1 site in 1 country36 target enrollmentStarted: June 15, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
36
Locations
1
Primary Endpoint
Amount of Crowding Relieved

Study Overview

Brief Summary

In recent times, many patients want their treatment duration to be reduced, because lengthy orthodontic treatment duration is associated with negative sequelae such as discomfort, pain, white spot lesions, and decreased patient's compliance. Several techniques have been employed in an attempt to accelerate the tooth movement and shorten the lengthy orthodontic treatment duration. So, this study will investigate the effectiveness of minimal invasive technique like piezocision and microosteoperforation in alleviating mandibular anterior crowding which is one of the common malocclusiom and provide scientific knowledge regarding which minimal invasive tecnique will relieve the crowding faster.

Detailed Description

Records will be taken from patients who are meeting selection criteria and then analysis of record will be done to attain a proper diagnosis and treatment plan. Afterthat, those patients will be referred to oral surgery department for extraction of first premolar. After healing, orthodontic treatment will be started with bonding of preadjusted MBT 0.022" slot straight wire appliance(Patient will be instructed to report immediately in case of breakage of appliance), after that, randomisation and allocation of two groups will be done and on the day of initial aligning archwire placement i.e., 0.014" NiTi, active interventions(piezocision and micro-osteoperforations) will be done for each group and then levelling and alignment will be continued with the following arch wire sequence 0.016" , 0.016" x 0.022" and 0.017" x 0.025" NiTi. Levelling and alignment will be considered finished when 0.017x0.025" NiTi archwire will be engaged passively in the brackets. Records i.e,. mandibular study models will be taken on the day of surgical procedure before surgery (T0) and then after every 4th week i.e., 4th week(T1), 8th week(T2), 12th week(T3), 16th week(T4). Following this, data collection and interpretation of results will be done. And also, CBCT will be taken at post levelling and alignment with 0.017" x 0.025" arch wire to assess the root resorption and marginal alveolar bone loss.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
16 Years to 25 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Patient satisfying the following criteria will be included in this clinical study:
  • •Patients with age between 16-25 years
  • •Patients with either Angle's class I or class II malocclusion with moderate crowding in the anterior mandible(LII- 4-6mm) who requires extraction in the lower arch (tooth-size-arch-length discrepancy>5 mm)
  • •Permanent dentition
  • •Existence of all tooth in the mandibular arch (except third molars which may or may not be present)
  • •Good oral hygiene and periodontal health
  • •No smoking habit.

Exclusion Criteria

  • •medical conditions that would affect tooth movement (corticosteroid treatments, NSAIDs consumption, bisphosphonates, hyperparathyroidism, osteoporosis, uncontrolled diabetes)
  • •Contraindication to oral surgery (medical, social, psychological)
  • •Missing tooth in the mandibular arch
  • •Presence of primary or supernumerary tooth in mandibular arch
  • •Previous orthodontic treatment
  • •Poor oral hygiene and current periodontal disease
  • •Smoking habit.

Arms & Interventions

GROUP - A: PIEZOCISION GROUP

Experimental

This group will receive piezocision using piezotome inbetween the roots of mandibular anteriors after the placement of initial arch wire.

Intervention: GROUP - A: PIEZOCISION GROUP (Procedure)

GROUP- B: MICRO-OSTEOPERFORATION GROUP

Experimental

This group will receive Micro-Osteoperforation using orthodontic mini-implants and mini-implant screw driver after the placement of initial arch wire.

Intervention: GROUP- B: MICRO-OSTEOPERFORATION GROUP (Procedure)

Outcomes

Primary Outcomes

Amount of Crowding Relieved

Time Frame: 16 weeks

Measured with Little Irregularity index using Digital caliper

Amount of Crowding Relieved

Time Frame: 4 weeks

Measured with Little Irregularity index using Digital caliper

Amount of Crowding Relieved

Time Frame: 8 weeks

Measured with Little Irregularity index using Digital caliper

Amount of Crowding Relieved

Time Frame: 12 weeks

Measured with Little Irregularity index using Digital caliper

Secondary Outcomes

  • Overall Alignment Time(16 weeks)
  • Marginal Alveolar Bone Loss(16 weeks)
  • Root resorption of mandibular anteriors(16 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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