Evaluation of the Effectiveness of Piezocision and Micro-osteoperforation in Alleviating Mandibul… (NCT04940351) | Clinical Trial Compass
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Evaluation of the Effectiveness of Piezocision and Micro-osteoperforation in Alleviating Mandibular Anterior Crowding
India36 participantsStarted 2021-06-15
Plain-language 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.
Who can participate
Age range16 Years – 25 Years
SexALL
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Inclusion criteria
✓. 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
✕
What they're measuring
1
Amount of Crowding Relieved
Timeframe: 4 weeks
2
Amount of Crowding Relieved
Timeframe: 8 weeks
3
Amount of Crowding Relieved
Timeframe: 12 weeks
4
Amount of Crowding Relieved
Timeframe: 16 weeks
Trial details
NCT IDNCT04940351
SponsorPostgraduate Institute of Dental Sciences Rohtak