To Compare and Evaluate the effectiveness of Synthetic Bone Graft Material with and without Injectable Human Blood Clot in the Treatment of Bony Defects in Chronic Gum Disease.
- Conditions
- Health Condition 1: K053- Chronic periodontitis
- Registration Number
- CTRI/2024/07/070436
- Lead Sponsor
- Dr Priyanka Dalvi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1) Patients in the age group of 30 to 60 years.
2) Patients diagnosed with Chronic Periodontitis.
3) Patients who are non smokers or do not consume tobacco in any other form.
4) Patients are in good systemic health with no contraindication to periodontal surgery.
5) Patients having pocket depths greater than 5mm, intraosseous defect greater than 3mm and with radiographic evidence of vertical/angular bone loss in the affected sites.
1) One-walled osseous defects.
2) Patients suffering from any systemic diseases or with a compromised immune system.
3) Patients who had received any type of periodontal therapy for the past 6 months.
4) Patients taking immunosuppressant drugs like corticosteroids.
5) Patients with a known history of allergy to Doxycycline or Chlorhexidine or any other medicine used in the study.
6) Patients showing unacceptable oral hygiene compliance during / after Phase I periodontal therapy.
7) Patients taking any drug known to cause gingival enlargement.
8) Pregnant and/or lactating mothers.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method