Comparative study to evaluate the efficacy of Chitosan(natural polymer) with and without synthetic bone material in treatment of periodontal disease(gum disease).
- Conditions
- Health Condition 1: K053- Chronic periodontitis
- Registration Number
- CTRI/2020/04/024808
- Lead Sponsor
- DR PREETI
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1. Patients of either sex diagnosed with chronic periodontitis in the age range of 18 to 60.
2. Patients who are systemically healthy.
3. Patient with intra-bony pocket measuring greater than 5mm with evidence of radiographic defect depth of greater than 2 mm.
4. Patients who are willing to comply with the study protocol and will be able to come for regular follow up.
1. Patients who have undergone periodontal therapy during the previous 6 months, or exhibit poor plaque control after phase I therapy.
2. History of any uncontrolled systemic disease such as diabetes mellitus, hypertension, osteoporosis, unstable or life-threatening conditions, bleeding disorder, undergoing antibiotic, anti-inflammatory or steroid therapy.
3. Current smokers.
4. Pregnant or lactating women.
5. Vegan/ vegetarians.
6. Patients with history of allergy to crustaceans
7. Patients contraindicated for periodontal therapy
8. Tooth with poor prognosis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Radiographic percentage defect fill <br/ ><br>2.Periodontal probing depth <br/ ><br>3.Clinical attachment level <br/ ><br>Timepoint: Baseline,3 months and 6 months
- Secondary Outcome Measures
Name Time Method 1.Gingival index <br/ ><br>2.Plaque indexTimepoint: Baseline,3 months and 6 months