A clinical and radiographic trial to study the treatment outcomes for bony defects using autograft VS combination of demineralized bone matrix and autograft.
- Conditions
- Health Condition 1: K053- Chronic periodontitis
- Registration Number
- CTRI/2023/11/059834
- Lead Sponsor
- ONE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.PRESENCE OF PERIODONTITIS WITH VERTICAL INTRABONY DEFECT HAVING PROBING POCKET DEPTH PPD MORE THAN OR EQUAL TO 5 MM, RADIOGRAPHIC DEFECT DEPTH MORE THAN OR EQUALTO 3MM AFTER PHASE I THERAPY.
2.ABSENCE OF ANY ANATOMICAL LIMITATIONS.
3.PATIENT WILLING TO UNDERGO SURGERY AND READY TO GIVE WRITTEN CONSENT.
1) Patients with systemic diseases, smokers and pregnant and lactating women.
2) Individuals with unacceptable oral hygiene.
3) Patients contraindicated for periodontal surgery.
4) Patients undergone periodontal therapy for past 6 months.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method COMPARE REDUCTION IN PROBING DEPTH FOR INTRABONY VERTICAL DEFECTSTimepoint: Baseline to 6 months
- Secondary Outcome Measures
Name Time Method ONETimepoint: NONE