Periodontal Disease Clinical Trial
Official title:
Comparative Evaluation of Porous and Non Porous Variants of Bioactive Glass in the Treatment of Periodontal Intrabony Defects: A Cone Beam Computed Tomography Analysis
Till date, no study has been reported in the literature where porous bioactive glass was used for the management of periodontal osseous defects. In this context, the present study is designed to assess the efficacy of the porous variant of bioactive glass and compare with that of nonporous variant using cone beam computed tomography.
OBJECTIVES:
1. To evaluate clinically the periodontal healing with Porous variant of Bioactive Glass
placed in the intra bony defects at an interval of 6 months.
2. To evaluate clinically the periodontal healing with Non Porous variant of Bioactive
Glass placed in the intra bony defects at an interval of 6 months.
3. To evaluate the radiographic changes in the intra bony defect grafted with Porous
variant of Bioactive Glass at baseline and an interval of 6 months.
4. To evaluate the radiographic changes in the intra bony defect grafted with Non Porous
variant of Bioactive Glass at baseline and an interval of 6 months.
5. To compare clinically soft tissue healing for sites grafted with Porous variant of
Bioactive Glass and sites grafted with Non Porous variant of Bioactive Glass in the
treatment of periodontal intra bony defects at an interval of 6 months.
6. To compare the radiographic changes for sites grafted with Porous variant and sites
grafted with Non Porous of Bioactive Glass in the treatment of periodontal intra bony
defects at an interval of 6 months.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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