Effect of combination of i-PRF and Xenograft in infrabony defect regeneratio
Not Applicable
- Conditions
- Health Condition 1: K053- Chronic periodontitis
- Registration Number
- CTRI/2022/03/041402
- Lead Sponsor
- A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients, who are cooperative, motivated and committed.
2. Patients with at least one tooth with periodontal probing depth (PD) >= 5mm when measured using a manual periodontal probe (UNC 15).
3. Radiographic presence of at least one infrabony osseous defect having depth >= 3 mm as measured.
4. Patients who will maintain optimum level of oral hygiene or full mouth plaque index score of <=1.
Exclusion Criteria
1. Patients with any known systemic disease/conditions and drug/ medication intake that will interfere with wound healing or minor surgical procedures.
2. Patients who are current smokers or consuming any other form of tobacco and not willing to quit.
3. Patients allergic to any drug and/or material, used in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method A.Clinical Parameter <br/ ><br>i.Pocket depth <br/ ><br>ii.Clinical attachment level <br/ ><br> <br/ ><br>B.Radiographic parameter <br/ ><br>i.Defect depth <br/ ><br>ii.Amount of defect fill <br/ ><br>iii.% of defect fill <br/ ><br>iv.Amount of defect resolution <br/ ><br>v. %of defect resolution <br/ ><br>Timepoint: baseline (after SRP) 3 months and 6 months
- Secondary Outcome Measures
Name Time Method i.Plaque Index <br/ ><br>ii.Bleeding index <br/ ><br>Timepoint: baseline ( after SRP), 3 months and 6 months