A Study to Compare and evaluate the effect of one sided gum surgery alone or in combination with Component of blood (PRF) in bony defects associated with gum disease.

Not Applicable

• Conditions: Health Condition 1: K053- Chronic periodontitisHealth Condition 2: null- Periodontitis (osseous defects)

• Registration Number: CTRI/2019/10/021752
• Lead Sponsor: MIDSR Dental college

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

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

Inclusion Criteria

1. Patient diagnosed with localized or generalized chronic periodontitis as per American

Academy of Periodontology International Workshop for Classifications of

Periodontal Disease 1999.

2. Subjects having acceptable systemic health.

3. Intrabony defect in both maxillary or mandibular region.

4. Patients having at least one intrabony defect more than or equal to 3 mm along with attendant pocket depth more than or equal to 5mm.

5. Absence of overt clinical inflammation at the time of surgery.

6. Patient signing written informed consent

Exclusion Criteria

1. Medically compromised patients.

2. With unacceptable oral hygiene (Plaque index >2)

3. With any metabolic disease or endocrine disease having direct or indirect influence on

Bone healing.

4. With any periapical pathology associated with endodontic infection in the region of

Interest.

5. Patient on active orthodontic treatment.

6. Patient having >4 mm pocket in selected tooth on mid oral or palatal aspect, requiring

Buccal as well as oral flap for access.

7. Pregnant and lactating women.

8. Presence of defective prosthesis in the area of interest.

9. Subjects who are smokers and consume tobacco in any form.

10. Patient who are using drugs that may cause gingival enlargement, those allergic or sensitive to any medications that will be used in the study.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Probing depth, Clinical attachment level <br/ ><br>Radiographic bone fill <br/ ><br>Timepoint: At 3 month and at 6 months <br/ ><br>

Secondary Outcome Measures

Name	Time	Method
Gingival marginal level, plaque index, gingival indexTimepoint: At 3month and at 6 months