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Essential Oils With and Without Alcohol: Substantivity and Antiplaque Effect

Essential Oils With and Without Alcohol: in Vivo Antibacterial Effect

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03146390
Enrollment
20
Registered
2017-05-09
Start date
2017-05-02
Completion date
2017-08-31
Last updated
2017-05-09

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

Conditions

Oral Biofilm, Dental Plaque, Periodontitis

Keywords

biofilms, essential oils, microscopy, confocal, mouthwashes

Brief summary

The Essential oils (EO) are composed by a wide diversity of products. Therefore, their antimicrobial activity will be related to their composition, configuration, amount and their possible interaction. The traditional formulation containing EO (T-EO) is a complex mixture of phenolic compounds combined with determinate EO: 0.092% of eucalyptol, 0.064% of thymol, 0.06% of methyl-salicylate and y 0.042% of menthol. All of this solved in a hydroalcoholic vehicle containing from a 21.6% to a 26.9% of alcohol. Thus, T-EO contain ethanol, which is a chemical compound used in order to dissolve and stabilize the numerous substances present in the rinse. The concentration of ethanol present in the T-EO rinses, as previously said, is more than 20%. This concentration of ethanol, higher than 20%, is been found sufficient to dissolve the EO but insufficient to have a direct antibacterial effect. In fact, the manufacturer presents the alcohol contain (21.6%), among others, as an inactive ingredient in its formula. Over the years, the adequacy of the use of ethanol in mouthwashes, as well as their effects on the surfaces of composite restorations and their possible role in development of oropharyngeal cancer have been discussed. Although a direct cause-and-effect correlation between the development of oropharyngeal carcinoma and the use of alcohol-based rinses has not been demonstrated and probably it will never be (at least by epidemiological studies), it is considered desirable to eliminate ethanol from daily mouthwashes, especially for those patients at higher risk. Furthermore, the fact that the alcohol is present in its formula, have produced that some clinical practitioners do not prescribe the traditional formula due to the controversy of the issue. All this have lead to the development of new, alcohol free formulations of EO (Af-EO). The composition of the Af-EO is exactly the same in their active ingredients (Eucalyptol, Thymol, Methyl-salycilate and Menthol), but sodium fluoride has been added. Some differences are found in their inactive ingredients. These are based on the alcohol containing of the T-EO, without presence in the Af-EO and the presence of Propylene Glycol, sodium lauryl sulfate and sucralose in the Af-EO, without presence in the T-EO. In order to measure the efficacy of a mouthwash against the dental plaque two different concepts should be defined: the substantivity and antiplaque effect. The substantivity of an oral antiseptic is defined as the prolonged adherence to the oral surfaces and its slow release at effective doses which guarantee the persistence of the antimicrobial activity. The more substantivity an oral antiseptic has the better. For its study in vivo, the most popular models are those which analyze the effect that a single mouthwash has in a mature biofilm. The second aspect that should be studied from an oral antiseptic, the antiplaque effect, is defined as the capacity that an agent has to avoid the formation of bacterial aggregates (plaque) on the oral surfaces. For its study in vivo, models start from a baseline sample with levels of plaque near to 0 in order to assess the power of the antiseptic to reduce the formation of bacterial plaque (normally dental plaque) against the control. A clinical study of 6 months using a determinate antiplaque agent is necessary in order to tag an antiseptic as effective. However, in the literature, there is an established model of 4 days of plaque regrowing which can assess the inhibitory activity that the mouthwashes have per se; furthermore, it determines the relative efficacy of the different formulations being considered as predictable of the antiplaque effect of an antiseptic. In addition, another important factor in the study in vivo of an oral antiseptic is the necessity to conserve intact the oral biofilm at all stages: formation, recollection and analysis of the oral samples. This is in order not to interfere the delicate three dimensional structure of the oral biofilm which has been proven to be essential in the resistance to the effects of an external antiseptic agent. For these reasons, the study of the oral biofilm with the help of intraoral disks hold in specially designed apparatus combined with the application of the Confocal Laser Scanning Microscopy have proved to be very valuable at the study of the oral biofilm in its intact hydrated natural state. Since an alcohol free formulation of the EO have come up to the market, it seems convenient to compare its effects to the traditional one. Although some studies comparing the effects of T-EO and Af-EO have been found, none of them assessed and compared their substantivity and antiplaque effect in an in vivo model of structured oral biofilm. For this reason, the aim of the present study was to compare the in vivo antibacterial effect (immediate effect, substantivity and antiplaque effect) of the EO with and without alcohol in structured oral biofilm.

Interventions

all subjects will perform all interventions of all arms

DRUGAlcohol free essential oils

all subjects will perform all interventions of all arms

OTHERWater

all subjects will perform all interventions of all arms

Sponsors

University of Santiago de Compostela
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Systemically healthy adults. * Minimum of 24 permanent teeth. * No gingivitis (Community Periodontal Index score = 0). * No periodontitis (Community Periodontal Index score = 0). * Absence of untreated caries.

Exclusion criteria

* Smoker or former smoker. * Presence of dental prostheses. * Presence of orthodontic devices. * Antibiotic treatment or routine use of oral antiseptics in the previous 3 months. * Presence of any systemic disease that could alter the production or composition of saliva.

Design outcomes

Primary

MeasureTime frameDescription
Change in the Bacterial viability (%) (substantivity)Baseline, 30 seconds, 1 hour, 3 hours, 5 hours and 7 hours after the single applicationratio of alive/dead bacteria
Bacterial viability (%) (antiplaque effect)10 hours after the last mouthwashratio of alive/dead bacteria
Change in the Biofilm Thickness (Microns) (substantivity)baseline, 30 seconds, 1 hour, 3 hours, 5 hours and 7 hours after the single applicationthickness of the biofilm from the base of the substrate to the top surface of the biofilm
Biofilm Thickness (Microns) (Antiplaque effect)10 hours after the last mouthwashthickness of the biofilm from the base of the substrate to the top surface of the biofilm
Covering Grade (%) (antiplaque effect)10 hours after the last mouthwasharea of the substrate that is covered by the biofilm after the 4 days of treatment

Countries

Spain

Contacts

Primary ContactInmaculada Tomás, Senior Lecturer
victor.quintas@usc.es+34981560031

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026