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se of Boric Acid Mouth rinse in decreasing Aerosols levels during Scaling

Phase 2
Completed
Conditions
Health Condition 1: K053- Chronic periodontitis
Registration Number
CTRI/2017/10/010189
Lead Sponsor
JSS Dental College Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
10
Inclusion Criteria

1.Subjects who are willing to give inform consent.

2.Subjects who are diagnosed with Chronic Generalised Periodontitis.[9]

3.Subjects who have at least 20 functional teeth.

4.A mean plaque index (PI) of at least 2-3.[10]

5. Subjects within the age range of 25-55 years.

6.Systemically healthy subjects.

7.No periodontal therapy including any non surgical or surgical therapy 6 months prior to the start of the study.

Exclusion Criteria

1.Subjects who are unwilling to give inform consent.

2.Subjects with respiratory infection.

3.Subjects who had received any chemotherapeutic mouth rinses and oral irrigation 6 months prior to the start of the study.

4.Subjects who had received any systemic or topical antibiotic therapy in past 6 months.

5.Hypersensitivity to Chlorhexidine gluconate or Boric acid and other formula ingredients.

6.Smokers.

7.Pregnant / Lactating women

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
efficacy of pre-procedural boric acid mouth rinse in Reducing Viable Bacteria in Dental Aerosols Produced during Ultrasonic ScalingTimepoint: 10 chronic periodontitis subjects will be enrolled for scaling in duration of 3 months
Secondary Outcome Measures
NameTimeMethod
to compare efficacy of boric acid and chlorhexidine mouthrinseTimepoint: 10 chronic periodontitis subjects will be enrolled in 3 months study duration .
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