Comparision of Two Different One-stage Full-mouth Disinfection Protocols by Assessing Dental Plaque and Tongue Coat in the Treatment of Chronic Periodontitis

Comparative Evaluation of Two Different One-stage Full-mouth Disinfection Protocols by Assessing Dental Plaque and Tongue Coat using N-Benzoyl-DL-Arginine-2-Naphthylamide Assay in the Treatment of Chronic Periodontitis - A Randomized Clinical Study.

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/05/013930

Enrollment

Registered

2018-05-17

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: 0.2% Chlorhexidine Mouthwash(Bollens Protocol for Full-mouth disinfection): 0.2% Chlorhexidine mouthwash for 2 weeks (Quirynen Protocol for Full-mouth dinsinfection)versus for two month

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subjects aged 18-60 years rendering informed consent. 2. Presence of minimum 20 natural scorable teeth excluding third molars. 3. Subjects diagnosed with chronic periodontitis based on American Academy of Periodontology (AAP) classification 1999. 4. Presence of at least two teeth per quadrant with a probing depth of > 3mm. 5. Subjects having good level of oral hygiene

Exclusion criteria

Exclusion criteria: 1. Subjects who have received any form of periodontal therapy, surgical or non-surgical within past 6 months. 2. Subjects who have received antibiotic and / or anti-inflammatory therapy within the past 3 months. 39 3. Subjects wearing orthodontic appliances. 4. Subjects suffering from any systemic disease. 5. Subjects who give present or past history of drug abuse. 6. Subjects who give present or past history of Smoking and tobacco consumption. 7. Subjects with untreated grossly carious teeth. 8. Subjects with severe abrasion of teeth. 9. History of known allergies to constituents found in the mouthrinse (0.2% chlorhexidine gluconate) or dentifrice assigned during the intervention. 10. Subjects with a habit of mouth breathing, para-functional habits like bruxism, clenching etc. 11. Subjects with lip piercing and tongue piercing. 12. Pregnant women and lactating mothers. 13. Physically debilitated subjects.

Design outcomes

Primary

Measure	Time frame
comparing dental plaque and tongue coat quantitatively through PI at 2 weeks and 6 weeks follow up from baseline, and through WTCI at 2 weeks and 8 weeks follow up from baseline; and qualitatively through BANA assay through BANA P and BANA T scores 8 weeks follow up.Timepoint: 8 weeks	—

Secondary

Measure	Time frame
assessment of healing outcomes of change in clinical parameters of GI, SBI, PD, RCAL and GR at 6 weeks from baselineTimepoint: 6 weeks	—

Countries

India

Contacts

Public ContactArjumand Farooqui

Department of Periodontics, MGM Dental College and Hospital, Navi Mumbai

drvinkin@gmail.com9769804390

Outcome results