A study to evaluate the efficacy of adding patients blood cells to a bone substitute in the treatment of bone loss observed in chronic periodontitis

Not Applicable

Completed

• Conditions: Health Condition 1: null- Periodontitis

• Registration Number: CTRI/2017/10/010118
• Lead Sponsor: Aravinda Basireddy

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2014-10-28
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 14

Inclusion Criteria

Patients with bilateral mandibular degree 2 furcation defects, which show evidence of bone loss in a intra oral peri apical radiography and are not endodontic ally involved, with a pocket depth of greater than or equal to 5mm

Exclusion Criteria

Any systemic illness affecting periodontal wound healing, smokers, pregnant and lactating mothers, allergic to medications

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Probing depth and clinical attachment level gainTimepoint: 3 months and 6 months

Secondary Outcome Measures

Name	Time	Method
Gingival margin level,Plaque I decided and sulcus bleeding indexTimepoint: 3 months 6 months;Radiography parameters 1)horizontal defect depth 2)vertical defect depth measured on a CBCTTimepoint: 6months