comparision of regular used suction tip with newly modified suction tip for control of spread of infective aerosol from ultrasonic scaling

Not yet recruiting

• Conditions: Chronic gingivitis,

• Registration Number: CTRI/2022/02/040010

Brief Summary

This study will be carried out in 30 sides(left/right) in 15 patients (split mouth) in biofilm induced gingivitis patients undergoingultrasonic scaling procedure. Patients meeting the inclusion criteria will beconsidered for the present study.

Selected patients will be divided into 2groups:

Group A (test side)- Ultrasonic scaling willbe done (on left or right half of the mouth) with an ultrasonic scaler, alongwith ingenious suction tip for 10 mins.

Group B (15 sides): - Ultrasonic scaling willbe done (on left or right half of the mouth) with an ultrasonic scaler withconventional suction tip for 10 mins.

**Procedure**

Biofilm inducedgingivitis patients ready forultrasonic scaling will be provided information about the study.

Informed verbal and written consent will beobtained from each subject.

Each study participant will act as his/her owncontrol and will be subjected to both the study group criteria.

Group A (15 sides): - Ultrasonic scaling willbe done (on left or right half of the mouth) with an ultrasonic scaler, alongwith ingenious suction tip for 10 mins.

Patient will be shifted to another operatoryfor remaining ultrasonic scaling of other half of the mouth.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2022-03-02
• Study Start: 2022-06-02

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Biofilm induced gingivitis 2.
• Age – 18-60 years.
• Patients who are voluntarily ready to be a part of study and give informed consent.

Exclusion Criteria

• 1.Patients with medical conditions contraindicating the use of ultrasonic scalers were excluded from the study.
• 2.Uncooperative patients.
• 3.Not willing to participate in the study.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
colony forming unit count test	after 48 hours colony forming unit will counted.

Secondary Outcome Measures

Name	Time	Method
not applicable	not applicable

Trial Locations

Locations (1)

MGV KBH Dental College, Nashik; 🇮🇳 Nashik, MAHARASHTRA, India

MGV KBH Dental College, Nashik

🇮🇳Nashik, MAHARASHTRA, India

Mallinath Jadhav

Principal investigator

9890141235

mallijadhav84@gmail.com