Health Condition 1: K053- Chronic periodontitis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Apparently healthy patient Patient age ranging 20to35years. Good oral hygiene (plaque score 0) Periodontal pocket less than or equal to 4mm. No radiographic evidence of interdental bone loss. The respective teeth should be free from caries with no fixed prosthesis or orthodontic appliances. Participants who will provide informed consent will be included in the study
Exclusion criteria
Exclusion criteria: Pregnancy and lactating mothers Tobacco users and alcoholic Patients with uncontrolled systemic conditions/disease Fixed restoration on study teeth Tooth mobility Consumption of drugs causing gingival hyperplasia. Interdental bone loss Inadequate attached gingiva on study teeth
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the clinical efficacy of papilla reconstruction using incision and submucosal mobilization ( PRISM) with and without platelet rich fibrin (PRF)Timepoint: Baseline 1 week 1 month 3 months 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the gain in interdental papilla fill achieved with the PRISM technique with platelet rich fibrin To assess the gain in interdental papilla fill achieved with the PRISM technique without platelet rich fibrin To compare the gain in interdental papilla fill achieved with PRISM technique with and without Platelet rich fibrin To determine the reduction in interdental black triangle height and width in PRISM technique with platelet rich fibrin. To determine the reduction in interdental black triangle height and width in PRISM technique without platelet rich fibrin. To compare the reduction in interdental black triangle height and width with and without Platelet rich fibrin To evaluate patient related outcomes after PRISM technique with and without platelet rich fibrin Timepoint: Baseline 1 week 1 month 3 months 6 months | — |
Countries
India
Contacts
KVG Dental College and Hospital