Antimicrobial Effect of Tropolone Containing Versus Tropolone Free Mouthwash

Trial statusRecruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age18-45
SponsorCairo University

About this trial

The objective of this study is to compare the effect of Tropolone containing mouthwash versus CHX 0.2% mouthwash in reducing intraoral microorganism. Randomized clinical trial study

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients should be between 18- 45 years of age.

All the volunteers participated in this study will be healthy looking with free medical history.

The volunteers will be asked to suspend their usual oral hygiene practice from two to four days before experiment studying.

Disqualifiers

Patients with a compromised medical condition.

Volunteers that receive any antimicrobial agent during at least two weeks prior to study.

Volunteer with fixed, removable prosthesis or orthodontics appliance.

Volunteers with DMF above six will be excluded.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Listerine total care zero

    Combination product

    reducing intra-oral cariogenic microorganism.

  • Chlorhexidine Mouthwash (0.2%).

    Combination product

    Chlorhexidine Mouthwash (0.2%).

Treatment groups

30 Participants
are divided into 2 treatment groups
Group A: Listerine total care zeroExperimental treatment 1 intervention
Group B: Chlorhexidine Mouthwash (0.2%).Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

Bacterial count.

viability counts of Mutans Streptococci lactobacilli

Time frame
Change from the baseline immediate after using mouthwash, at one week after mouthwash and at two weeks after regular use of mouthwash

Secondary outcomes

Other outcomes

Sponsors and contacts

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