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A clinical trial to Compare clinical and imaging evaluation in surgicalextraction of third molar teeth using two different surgical techniques

Phase 3
Conditions
Health Condition 1: M270- Developmental disorders of jaws
Registration Number
CTRI/2022/10/046244
Lead Sponsor
DIV OF ORAL AND MAXILLOFACIAL SURGERY AFMC PUNE
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Clinical and radiological diagnosis of all Horizontally impacted mandibular third molar (Winterââ?¬•s Sub-Classification).

Both male and female patients aged between 18 and 35 years of age

Exclusion Criteria

All Mesioangular,Vertical and Distoangular impacted mandibular third molars (Winterââ?¬•s classification)

Forceps extractions not requiring osteotomy

Any pathological condition that may affect bone healing

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the clinical outcome based on Pain assesed on Visual Analog Scale (VAS),Maximum inter-incisal mouth opening in millimetres and duration of the procedure recorded in minutes in patients undergoing surgical extraction of mandibular third molars using Piezosurgery unit and conventional rotary instrumentsTimepoint: After 7 days
Secondary Outcome Measures
NameTimeMethod
1. To compare the bone density using Cone Beam Computed Tomography in HOUSEFIELD UNITS formed in the extraction socket after surgical extraction of horizontally impacted mandibular 3rd molars using Piezoelectric unit and conventional rotary technique <br/ ><br> <br/ ><br>2.To compare the complication rate in surgical extraction of horizontally impacted mandibular 3rd molars using Piezoelectric unit and conventional rotary techniqueTimepoint: After 12 months
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