Health Condition 1: null- Chronic Periodontitis Patients
Conditions
Interventions
Intervention1: The trial is an Interventional trial in the treatment of chronic periodontitis comparing two different treatment modalities one involving the placement of Anorganic Bone Matrix/Cell Bin
Sponsors
None
Eligibility
Inclusion criteria
Inclusion criteria: 1.Presence of at least 2 radiographically detectable interproximal osseous defects with a probing depth >=5mm & clinical attachment loss >= 5mm following initial therapy. 2. The depth of the intraosseous component of the defect estimated as >=3mm by clinical and radiographic means.
Exclusion criteria
Exclusion criteria: 1. Subjects with history of systemic diseases, allergies or drug usage. 2. Subjects who have undergone periodontal treatment in previous 6 months 3. Teeth exceeding class II mobility.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcomes: Improvement in Periodontal Status i.e. reduction in Probing Pocket Depth, gain in Clinical Attachment Level, Bone Fill in Periodontal Infrabony Defect (seen radiographically)Timepoint: outcome will be assessed at 3 months and 6 months. | — |
Secondary
| Measure | Time frame |
|---|---|
| Reduction in Plaque scores and Gingival Bleeding scores representing improvement in Gingival (soft tissue) statusTimepoint: At 6 months | — |
Countries
India
Contacts
Public ContactDr. Abhay P. Kolte
V.S.P.M Dental College & Research Centre
Outcome results
None listed