This study measures the main outcome of tooth movement during orthodontic treatment using two different types of interventions one is I-PRF and another is L-PRF.
Not Applicable
- Conditions
- Health Condition 1: K089- Disorder of teeth and supporting structures, unspecified
- Registration Number
- CTRI/2024/07/070019
- Lead Sponsor
- KAVINKUMAR K A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Healthy individuals of both genders in the age group of 18 to 30 years.
2.Class I malocclusion with bimaxillary protrusion with average growth pattern.
Exclusion Criteria
1.Patients with systemic diseases like Bronchial Asthma, Hypertension, Diabetes, Epilepsy, Congenital heart disease, chronic liver disease, Juvenile Rheumatoid Arthritis, G-6PD deficient individuals, Gastrointestinal problems, Bleeding disorders.
2.Pregnant patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To measure the rate of tooth movement.Timepoint: T0 (at the start of retraction) <br/ ><br> T1 (2nd week) <br/ ><br> T2 (4th week) <br/ ><br> T3 (8th week) <br/ ><br> T4 (12th week) <br/ ><br> T5 (16th week)
- Secondary Outcome Measures
Name Time Method To measure the outcome of pain, at the time of tooth movement.Timepoint: T0 (at the start of retraction) <br/ ><br> T1 (2nd week) <br/ ><br> T2 (4th week) <br/ ><br> T3 (8th week) <br/ ><br> T4 (12th week) <br/ ><br> T5 (16th week)