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Evaluation of the efficacy of a new instrument for the oral hygiene

Comparative evaluation of the efficacy of a new instrument "the digital brush" for the oral hygiene in healthy young patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12613001308785
Enrollment
58
Registered
2013-11-25
Start date
2013-05-06
Completion date
2013-10-11
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Using a double-blind, randomized design, the oral hygiene condition of 30 young healthy volunteers using the new instrument "digital brush" associated with toothbrushing will be compared with the oral hygiene condition of 30 participants using mouth rinse associated with toothbrushing.

Interventions

Arm 1: the experimental group receives instructions to perform at "home" oral hygiene twice a day, for 2 weeks, using a toothbrush associated with a new instrument "the digital brush"(consisting on a gauze soaked with chlorhexidine and rolled up on the finger). Oral hygiene conditions of participants will be evaluted after 2 weeks. Details: The gauze contains 0,12% chlorhexidine; a) participants rolled up the gauze on the index finger, using rotative mouvements from gums to teeth; the gauze was

Arm 1: the experimental group receives instructions to perform at "home" oral hygiene twice a day, for 2 weeks, using a toothbrush associated with a new instrument "the digital brush"(consisting on a gauze soaked with chlorhexidine and rolled up on the finger). Oral hygiene conditions of participants will be evaluted after 2 weeks. Details: The gauze contains 0,12% chlorhexidine; a) participants rolled up the gauze on the index finger, using rotative mouvements from gums to teeth; the gauze was used only once; b) duration of 30 sec.; c) adherence is improved with 1-instructions made to the participants; 2-explanatory demonstration of its use during the first appointment; 3-daily patient diary.

Sponsors

Polytechnic University of Marche, Section of Stomatology
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

Enrollment of the participants will be performed at the Polytechnic University of Marche (Ancona, Italy), including healthy subjects aging between 18 and 35, good physical health, smokers and not

Exclusion criteria

Important periodontal disease; periodontal surgery within the previous 6 months; ongoing treatment with antibiotics and/or anti-inflammatory drugs; pregnancy or lactation; chronic systemic disease

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026