Assessment of bone formation ability of demineralized tooth matrix and injectable platelet rich fibrin flowable graft material using- An IN-vivo study
Phase 4
- Conditions
- Health Condition 1: K082- Atrophy of edentulous alveolar ridge
- Registration Number
- CTRI/2024/04/065101
- Lead Sponsor
- I
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Teeth extracted for periodontal purpose (Grade 2 & 3 mobility)
Exclusion Criteria
Infected and decayed tooth and root canal treated tooth
2. Uncontrolled diabetes mellitus, Hypertension, Heavy smokers
3. Pregnant and lactating women
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Bone formation in the tooth socket filled with autogenous graft and comparing with BIO-OSSE using cone beam computed tomography and if patients are willing to consent bone histological study after implant placementTimepoint: Baseline, 3 months
- Secondary Outcome Measures
Name Time Method To compare the bone formation between the study groups at the end of the studyTimepoint: 03 months