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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02463006
Other study ID # DYPDCH/12/PG16
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received May 29, 2015
Last updated June 2, 2015
Start date January 2014
Est. completion date May 2015

Study information

Verified date June 2015
Source Dr. D. Y. Patil Dental College & Hospital
Contact n/a
Is FDA regulated No
Health authority India: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date May 2015
Est. primary completion date September 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- INCLUSION CRITERIA

1. Age: 18-55 years.

2. Probing Depth >5mm.

Exclusion Criteria:

- EXCLUSION CRITERIA

1. History of periodontal treatment last six months.

2. Bleeding disorders.

3. Gross oral pathology.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Intervention

Drug:
Porous variant of Bioactive Glass.
Flap surgery with Porous variant of Bioactive Glass.
Non porous variant of Bioactive Glass.
Flap surgery with non-Porous variant of Bioactive Glass.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Dr. D. Y. Patil Dental College & Hospital

References & Publications (2)

Gokhale ST, Dwarakanath CD. The use of a natural osteoconductive porous bone mineral (Bio-Oss™) in infrabony periodontal defects. J Indian Soc Periodontol. 2012 Apr;16(2):247-52. doi: 10.4103/0972-124X.99270. — View Citation

Wohlfahrt JC, Aass AM, Rønold HJ, Heijl L, Haugen HJ, Lyngstadaas SP. Microcomputed tomographic and histologic analysis of animal experimental degree II furcation defects treated with porous titanium granules or deproteinized bovine bone. J Periodontol. 2 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change in relative attachment loss 6 months No
Secondary Change in probing depth 6 months No
Secondary Change in plaque index 6 months No
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