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Study of Growing Biofilm by an Antiplaque Mouthrinse

NCT00838266 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2009-09-23

No results posted yet for this study

Summary

The objective of this study is to evaluate the efficiency of a new mouthrinse on dental plaque deposits.

The study is carried out on 50 volunteers that are asked to use the mouthrinse without any other oral hygiene measure, during 4 days. It is a double bind, cross-over, randomized design: the same subjects test the active product and the placebo.

Conditions

  • Dental Plaque

Interventions

DRUG

mouthrinse (Grape Seed Extract + nicomethanol fluorhydrate)

Antiplaque mouthrinse containing active component three times a day, during 1 minute, for 4 days

OTHER

mouthrinse containing non-active component

Antiplaque mouthrinse containing non-active component three times a day, during 1 minute, for 4 days

Sponsors & Collaborators

  • University Hospital, Bordeaux

    lead OTHER

Principal Investigators

  • Cécile BADET, MD · University Hospital, Bordeaux

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-02-28
Primary Completion
2009-03-31
Completion
2009-03-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00838266 on ClinicalTrials.gov