A clinical trial to study the effect of scaling and root planing, scaling and root planing with diode laser, scaling and root planing with diode laser with the application of injectable platelet rich fibrin in the management of Periodontitis

Phase 4

Completed

• Conditions: Chronic periodontitis,

• Registration Number: CTRI/2024/04/066237

Brief Summary

Aim of the study is to compare the effect of Diode Laser and the application of injectable-Platelet rich fibrin as an adjunct to scaling with scaling alone in terms of reduction in Clinical Attachment Loss, Periodontal probing depth and Bleeding on probing. All the participants will be explained about the need, design of study. Informed written consent will be obtained from the patients. Clinical case history will be recorded. All the clinical parameters (CAL, PPD, BOP) will be recorded at baseline using UNC 15 periodontal probe (Hu Friedy). Each patient will undergo ultrasonic scaling (EMS) by a single operator. It is a single blind study in which the patient will be randomly assigned to Diode Laser application and Injectable-Platelet rich fibrin as an adjunct to scaling or scaling alone using “Computer generated†method. Patients will be instructed to follow the standard advised oral hygiene measures. The subjects will be re-evaluated for the CAL, PPD, BOP after 7 days . All the clinical parameters will be recorded at baseline and after 7 days by second blinded operator.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2024-07-23
• Study Start: 2024-10-05

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 15

Inclusion Criteria

• Patients with good general health in the age group of 30-70 years.
• Both Male and Female patients with chronic periodontitis.
• Probing depth ≥5 and <7 mm.
• Presence of atleast one periodontal pocket each any of the three quadrants.
• No furcation involvement.
• Patient willing to give informed consent.

Exclusion Criteria

• Major systemic illness 2.
• Confirmed or suspected intolerance to test products 3.
• Use of antibiotics drugs for the last 6 months 4.
• Heavy Smoking 5.
• Immunosuppressive chemotherapy 6.
• Pregnancy 7.
• Undergone any periodontal therapy.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduction in clinical attachment loss probing depth bleeding on probing	Baseline to six months

Secondary Outcome Measures

Name	Time	Method
Reduction in bleeding on probing	Baseline to six months

Trial Locations

Locations (1)

SMBT Dental college and hospital; 🇮🇳 Ahmadnagar, MAHARASHTRA, India

SMBT Dental college and hospital

🇮🇳Ahmadnagar, MAHARASHTRA, India

Dr Prachi Sarage

Principal investigator

9665203740

prachisarage696@gmail.com