Overview

Effect of Alendronate With β - TCP Bone Substitute in Surgical Therapy of Periodontal Intra-osseous Defects.

Status:
Completed
Trial end date:
2016-04-01
Target enrollment:
0
Participant gender:
All
Summary
The aim of the present study was to evaluate the bone formation potential of 400µg alendronate delivered in β-TCP in the treatment of periodontal intra-osseous defects.
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Panineeya Mahavidyalaya Institute of Dental Sciences & Research Centre
Treatments:
Alendronate
Criteria
Inclusion Criteria:

- Systemically healthy patients having an intra-osseous defect with probing depth ≥ 7mm
at baseline, presence of a ≥ 4mm vertical inter-proximal bone defect with at least one
bony wall after surgical debridement and with no history of previous periodontal
therapy were included into the study

Exclusion Criteria:

- Patients with known systemic diseases, aggressive periodontitis, smoking habit, known
or suspected allergy to bisphosphonates, pregnant and lactating women, study tooth
exhibiting tooth mobility greater than grade II and class III furcation defect were
excluded from the study.