UnknownPhase 4

Assessment of Inhibition of Biofilm Formation and Plaque Bacterial Count of Fluoride Varnish Containing Chlorhexidine and Cetylpyridinium Chloride Versus Conventional Fluoride Varnish

Egypt34 participantsStarted 2020-02-01

Plain-language summary

Two different Fluoride varnish systems(Fluoride varnish containing Chlorhexidine and Cetylpyridinium Chloride (CPC) and conventional fluoride) will be applied to high caries risk patients to assess their clinical effects on plaque accumulation and plaque bacterial count .

Who can participate

Age range18 Years – 40 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: Patients with good general state of health. * No signs of periodontitis. * Patients had a recorded high bacterial count after caries risk assessment. * No antibiotic treatment within 1 month prior to the start of the trial. * No current medication with anti-inflammatory drugs. * No use of antiseptic mouth rinses. * Non-smokers. Exclusion Criteria: * Patients with disabilities, systemic disease or severe medical conditions. * Patients with severe or active periodontal disease. * Antibiotic treatment within 1 month prior to the start of the trial. * Current medication with anti-inflammatory drugs.

What they're measuring

Plaque Retention

Timeframe: Patient will be evaluated at 2nd week of the study in the morning before teeth brushing.

Plaque Retention

Timeframe: Patient will be evaluated at 4th week of the study in the morning before teeth brushing.

Plaque Retention

Timeframe: Patient will be evaluated at 12th week of the study in the morning before teeth brushing.

Plaque Retention

Timeframe: Patient will be evaluated at 24th week of the study in the morning before teeth brushing.

Trial details

NCT IDNCT04254835

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2020-07-01

Contact for this trial

Hadeer H Mohamed

01015779373 hadeer.hesham91@gmail.com

View on ClinicalTrials.gov More High Caries Risk Patients trials

Who can participate

Age range18 Years – 40 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Plaque Retention

Timeframe: Patient will be evaluated at 2nd week of the study in the morning before teeth brushing.

Plaque Retention

Timeframe: Patient will be evaluated at 4th week of the study in the morning before teeth brushing.

Plaque Retention

Timeframe: Patient will be evaluated at 12th week of the study in the morning before teeth brushing.

Plaque Retention

Timeframe: Patient will be evaluated at 24th week of the study in the morning before teeth brushing.