comparison of two different plating systems for fracture of the lower jaw
Not Applicable
- Conditions
- Health Condition 1: K088- Other specified disorders of teethand supporting structures
- Registration Number
- CTRI/2021/02/031495
- Lead Sponsor
- SGT Dental college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All patients irrespective of gender.
Patients above 16 years of age.
All partially and complete dentulous patients with non comminuted mandibular fractures of
Symphysis, Parasymphysis, Body and Angle.
Patients with fairly good general health condition according to American society of
Anesthesiologists classification (ASA- I and II) fit to undergo fracture treatment under GA/LA.
Exclusion Criteria
Medically compromised patients (ASA 3 AND ASA 4) will not be included.
Patients with communited fractures and fractures in sagittal plane.
Edentulous patients.
Patients with known history of allergy to titanium.
5. Any other associated fractures of the facial skeleton involving occlusion.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the outcomes in patients undergoing Open <br/ ><br>reduction & Internal Fixation for Mandibular fractures with conventional miniplates and 3 <br/ ><br>Dimensional miniplates. <br/ ><br>Timepoint: clinical evaluation at immediate post op, 7 days, 1 month, 3 months <br/ ><br>radiographic evaluation at immediated postop and at 1 month
- Secondary Outcome Measures
Name Time Method To clinically Measure the bite force generated preoperatively and postoperatively. <br/ ><br>To clinically evaluate post-operative mouth opening. <br/ ><br>To clinically evaluate protrusive and laterotrussive movements. <br/ ><br>To clinically assess the stability of the post-operative intercuspation based on the need for <br/ ><br>post-operative IMF/IME. <br/ ><br>To radiographically assess post-operative hardware failure. <br/ ><br>To radiographically check the degree of reduction achieved (distraction at lower border).Timepoint: Clinical evaluation at immediate post op 7 days 1 month 3 months <br/ ><br>Radiographic evaluation at immediated postop and at 1 month