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Comparision of blood product and polymer solution included blood product for the treatment of jaw joint problem.

Not Applicable
Conditions
Health Condition 1: M248- Other specific joint derangements,not elsewhere classified
Registration Number
CTRI/2023/11/059991
Lead Sponsor
Malya Manoj Kumar Naik
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Patients in the age group of 18-60 years.

2.Patients diagnosed with Wilkes stage II and III of ID of temporomandibular joint.

3.Patients not responding to conservative treatments.

4.Willingness to participate in the study and to give informed consent.

5.Willing for a minimum 6-month follow-up after undergoing treatment.

Exclusion Criteria

1.Any systemic or malignant disease that could interfere with the TMJ treatment or assessment.

2.History of Previous TMJ surgery/condylar trauma.

3.Failure during intra-articular injection procedure.

4.Fibrous or osseous ankylosis of the TMJ.

5.Cutaneous, otic, or articular infections.

6.Edentulous patients.

7.Pregnant and breastfeeding.

8.Bilateral TMJ pain.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Pain at rest & chewing, assessed by means of a visual analog scale. <br/ ><br>2.Mandibular range of movement, comprising maximum non assisted & assisted mouth opening, left & right laterotrusion, & protrusion movements. <br/ ><br>3.Clicking by Auscultation. <br/ ><br>4.QOL questionnaire. <br/ ><br>5.Functional limitation during usual jaw movements.Timepoint: 1.Pain at rest & chewing at 1 Week,1 month,3 months,6 months postoperative. <br/ ><br>2.Mandibular range of movement, comprising maximum non assisted & assisted mouth opening, left & right laterotrusion, & protrusion movements at 1 Week,1 month,3 months,6 months postoperative. <br/ ><br>3.Clicking at 1 Week,1 month,3 months,6 months postoperative. <br/ ><br>4.QOL questionnaire at 1 Week,1 month,3 months,6 months postoperative. <br/ ><br>5.Functional limitation at 1 Week,1 month,3 months,6 months postoperative.
Secondary Outcome Measures
NameTimeMethod
1.Pain at rest & chewing, assessed by means of a visual analog scale. <br/ ><br>2.Mandibular range of movement, comprising maximum non assisted & assisted mouth opening, left & right laterotrusion, & protrusion movements. <br/ ><br>3.Clicking by Auscultation. <br/ ><br>4.QOL questionnaire. <br/ ><br>5.Functional limitation during usual jaw movements.Timepoint: 1.Pain at rest & chewing at 1 Week,1 month,3 months,6 months postoperative. <br/ ><br>2.Mandibular range of movement, comprising maximum non assisted & assisted mouth opening, left & right laterotrusion, & protrusion movements at 1 Week,1 month,3 months,6 months postoperative. <br/ ><br>3.Clicking at 1 Week,1 month,3 months,6 months postoperative. <br/ ><br>4.QOL questionnaire at 1 Week,1 month,3 months,6 months postoperative. <br/ ><br>5.Functional limitation at 1 Week,1 month,3 months,6 months postoperative.
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