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Clinical Trial Summary

To demonstrate the absence of irritation potential (primary dermic irritability and cumulated dermic irritability) and allergy (sensibilization) of the product Dermacyd Breeze (Lactic Acid) Pocket BR.


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


NCT number NCT00784121
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 3
Start date October 2008

See also
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Completed NCT00783640 - Dermacyd Femina (Lactic Acid) Pocket BR - Photo Evaluation Phase 3
Completed NCT00783861 - Dermacyd Femina (Lactic Acid) Pocket BR - Compatibility Phase 3
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Completed NCT00793026 - Dermacyd Breeze Pocket BR (Lactic Acid) - Acceptability Phase 3
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