Study for Dermatological Evaluation of Topic Compatibility (Primary and Accumulated Dermical Irritability, Dermical Sensitivity) of Dermacyd Femina Pocket BR.
Sponsor study identifier
interventional
54
1 country
1
Study Start
October 2008
Date type not reportedThis date has not been verified as actual or estimated.
Primary Completion
November 2008
Actual (reported)Study Completion
Not reported
Date not reportedTo demonstrate the absence of irritation potential (primary dermic irritability and cumulated dermic irritability) and allergy (sensibilization) of the product Dermacyd Femina (Lactic Acid) Pocket BR.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
Not reported
Date not reportedClick on a node to explore related trials.
Some registry-reported names shown below are not yet linked in this graph.
Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
October 2008
Date type not reportedThis date has not been verified as actual or estimated.
October 31, 2008
Actual (reported)November 2008
Actual (reported)November 3, 2008
Actual (reported)The absence of primary and accumulated dermical irritability and dermical sensitivity will be evaluated using International Contact Dermatitis Research Group (ICDRG) scale.
Throughout the study
Lactic Acid (Dermacyd Femina)
Lactic Acid (Dermacyd Femina)
Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.
Sanofi-Aventis Administrative Office
São Paulo, Brazil
Jaderson Lima
Sanofi
54 participants (actual enrollment reported by the registry).
First Submitted
October 31, 2008
First Posted
November 3, 2008
Study Start
October 2008
Date type not reportedThis date has not been verified as actual or estimated.
Dermacyd PH_DETINBACK Tangerine Mix (Lactic Acid) - Safety.
Contact the study team to confirm eligibility.
Primary Completion
November 2008
Actual (reported)Last Updated
December 19, 2008
Record last verified: 2008-12
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Source: ClinicalTrials.gov.
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