To Compare the effectiveness of platelet concentrate with two different bone graft material for the periodontal defect in huma

Phase 3

• Conditions: Health Condition 1: K053- Chronic periodontitis

• Registration Number: CTRI/2022/09/045318
• Lead Sponsor: Dr Aishwarya Rathod

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 16 October 2023

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1.Systematically healthy patient.

2.Following initial therapy, presence of minimum 1 or 2 interproximal infrabony osseous defect PPD = 5mm and CAL = 5 and which are radiographically noticeable.

3.Clinically and radiographically there should be = 3mm defect depth which is affirmed on intrasurgical measurement.

4.A radiographically determined defect base should be minimum of 3 mm above the apex of the tooth

5.Presence of minimum =2mm zone of keratinized gingiva to permit total soft tissue coverage of the defect area.

Exclusion Criteria

1.Patient diagnosed with aggressive periodontitis.

2.Patients with poor oral hygiene care (Plaque Index >1)

3.Patients using tobacco in any form .

4.Involved tooth with inadequate root canal therapy and subsequent restoration

5.Involved tooth having mobility greater than grade II ,or defect extending in to furcation and third molars .

6.Prior history of periodontal surgery of the selected segment.

7.Females who are pregnant or lactating.

8.There is clinical and radiographic sign of untreated acute infection at the selected site, root fracture,apical pathology ,severe root irregularities, cemental pearls, cementoenamel projections, untreated carious lesion on root surface.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Radiographic Bone Fill In Infrabony Defects at 6 Month Post Surgery.Timepoint: Radiographic Bone Fill In Infrabony Defects at 6 Month Post Surgery.

Secondary Outcome Measures

Name	Time	Method
Gain in Clinical Attachment Level( CAL) <br/ ><br>Reduction In Probing Pocket Depth (PPD)Timepoint: 6 Months