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Efficacy of a Triclosan Formulation to Control the Initial Subgingival Biofilm Formation

NCT02192060 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2014-07-16

No results posted yet for this study

Summary

The aim of the study is to compare the effect of a suspension containing Triclosan in dynamic of the subgingival biofilm formation versus a Placebo suspension. The initial subgingival biofilm formation will be evaluated by means of Plaque Free Zone (PFZ).

Conditions

  • Dental Plaque

Interventions

OTHER

Test - Using of a suspension containing Triclosan

The participants should have used only the suspension containing Triclosan during 5 days and have stopped with their biofilm control homemade procedures.

OTHER

Control - Using of a suspension without Triclosan

The participants should have used only the Placebo suspension during 5 days and have stopped with their biofilm control homemade procedures.

Sponsors & Collaborators

  • Federal University of Rio Grande do Sul

    lead OTHER

Principal Investigators

  • Rui V. Oppermann, DDS, PhD · Federal University of Rio Grande do Sul

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-05-31
Primary Completion
2013-06-30
Completion
2013-06-30

Countries

  • Brazil

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 NCT02192060 on ClinicalTrials.gov