Sanofi-Aventis Administrative Office
São Paulo, Brazil
NCT Number: NCT00933712
Primary Objective:
To demonstrate the absence of irritation potential (primary dermic irritability and cumulated dermic irritability) and allergy (sensibilization) of the product Dermacyd Silver Floral
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Notify Me18 year–60 year
All sexes
Interventional
Phase 3
São Paulo, Brazil
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Dermacyd Silver Floral (Lactic Acid) sample will be applied like a curative for 6 weeks.
Time frame: from the treatment start to the end of the study (treatment period 6 weeks)
Sanofi
Industry
Study for Dermatological Evaluation of Topic Compatibility. Primary and Accumulated Dermical Irritability and Dermical Sensitivity for the Product Dermacyd Silver Floral (Lactic Acid).
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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