Comparision of treatment of bony defect with bone graft versus bone graft autologus blood product.

Phase 4

Completed

• Conditions: Health Condition 1: K053- Chronic periodontitis

• Registration Number: CTRI/2021/02/031327
• Lead Sponsor: MM College of Dental Sciences and Research

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2021-11-08
• Last Update Posted: 17 October 2022

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 45

Inclusion Criteria

Patients with chronic periodontitis exhibiting intrabony defects.

Exclusion Criteria

Patients with contraindication to periodontal surgery & local anesthesia.

Any systemic disease affecting the bone density and outcome of periodontal therapy.

Smokers, alcoholics, and patients with other adverse habits.

Pregnant, nursing and menopausal women.

Any known allergy/ hypersensitivity to any product used in this study.

Patients on long-term systemic therapy (antibiotics, anti-inflammatory bisphosphonates, hormonal replacement therapy and any other), taking any drug known to have periodontal implications that may interfere with wound healing.

Patients taking any anti-platelet and anticoagulant medication.

Patients who have undergone periodontal treatment within a period of past 1 year.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
radiographic bone fillTimepoint: baseline,6 months

Secondary Outcome Measures

Name	Time	Method
clinical attachment levelTimepoint: baseline,6 months;probing pocket depthTimepoint: baseline,6 months