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Sponsored by: |
Sanofi-Aventis |
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Information provided by: | Sanofi-Aventis |
ClinicalTrials.gov Identifier: | NCT00687037 |
To prove the safety, in normal conditions, of the odontological use formulation of the product Cepacol Canela Power.
Condition | Intervention | Phase |
---|---|---|
Healthy |
Drug: Cetylpyridinium chloride |
Phase III |
Study Type: | Interventional |
Study Design: | Supportive Care, Open Label, Uncontrolled, Single Group Assignment, Safety Study |
Official Title: | Uni Centric Study, Phase III, for Safety Oral Mucosa Evaluation: Basic Acceptability With Odontological Follow up - Cepacol Canela Power |
Enrollment: | 30 |
Study Start Date: | December 2007 |
Primary Completion Date: | February 2008 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
---|---|
I: Experimental
Cetylpyridinium chloride during 21 days.
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Drug: Cetylpyridinium chloride |
Ages Eligible for Study: | 18 Years to 60 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
Responsible Party: | sanofi-aventis ( Medical Affairs Study Director ) |
Study ID Numbers: | CPYRY_L_03930 |
Study First Received: | May 27, 2008 |
Last Updated: | May 29, 2008 |
ClinicalTrials.gov Identifier: | NCT00687037 |
Health Authority: | Brazil: National Health Surveillance Agency |
oral hygiene |
Benzocaine Cetylpyridinium Healthy |
Anti-Infective Agents Anti-Infective Agents, Local Therapeutic Uses Pharmacologic Actions |