NCT00497783|CompletedPhase 4
Acceptability Lactoserum (Dermacyd Delicata - New Fragrance)
Safety Dermatological Evaluation of the Acceptability With Gynecological Follow up for Dermacyd Femina Delicata
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Safety Dermatological Evaluation of the Acceptability With Gynecological Follow up for Dermacyd Femina Delicata
Sponsor study identifier
interventional
30
1 country
1
Study Start
May 2007
Date type not reportedThis date has not been verified as actual or estimated.
Primary Completion
Not reported
Date not reportedStudy Completion
Not reported
Date not reportedThe purpose of this study is to demonstrate the safety of the gynecological formulation in normal and usual usage condition of Dermacyd Femina Delicata.
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.
May 2007
Date type not reportedThis date has not been verified as actual or estimated.
July 6, 2007
Actual (reported)July 9, 2007
Actual (reported)Clinical and local tolerability
21 days
Adverse events and their association with the treatment.
21 days
Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.
Sanofi-aventis
São Paulo, Brazil
Jaderson Lima
Sanofi
First Submitted
July 6, 2007
First Posted
July 9, 2007
Study Start
May 2007
Date type not reportedThis date has not been verified as actual or estimated.
Last Updated
May 20, 2008
Record last verified: 2008-05
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Source: ClinicalTrials.gov.
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Source retrieved:
Topic Compatibility Dermacyd Wipes - Lactoserum - Hygiene
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