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Efficacy of Two Chlorhexidine Solutions to Control the Initial Subgingival Biofilm Formation

NCT02656251 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 35

Last updated 2016-01-14

No results posted yet for this study

Summary

The aim of the study is to compare the effect of a suspension containing chlorhexidine and alcohol and another one containing clorhexidine with no alcohol 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

DRUG

0.12% Clorhexidine with alcohol

Use of 0.12% Clorhexidine with alcohol every 12 hours for 04 days

DRUG

placebo

Use of placebo every 12 hours for 04 days

DRUG

0.12% Clorhexidine without alcohol

Use of 0.12% Clorhexidine without alcohol, every 12 hours for 04 days

Sponsors & Collaborators

  • Federal University of Rio Grande do Sul

    lead OTHER

Principal Investigators

  • Patricia Weidlich, PhD · Federal University of Rio Grande do Sul

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2015-07-31
Primary Completion
2015-12-31
Completion
2015-12-31

Countries

  • Brazil

Study Locations

More Related Trials

Entities

Drugs

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 NCT02656251 on ClinicalTrials.gov