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Clinical Trials/NCT00784121
NCT00784121
Completed
Phase 3

Study for Dermatological Evaluation of Topic Compatibility (Primary and Accumulated Dermical Irritability, Dermical Sensitivity) of Dermacyd Breeze Pocket BR.

Sanofi1 site in 1 country54 target enrollmentOctober 2008
ConditionsHygiene
InterventionsLactic Acid

Overview

Phase
Phase 3
Intervention
Lactic Acid
Conditions
Hygiene
Sponsor
Sanofi
Enrollment
54
Locations
1
Primary Endpoint
The absence of primary and accumulated dermical irritability and dermical sensitivity will be evaluated using International Contact Dermatitis Research Group (ICDRG) scale.
Status
Completed
Last Updated
17 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
October 2008
End Date
November 2008
Last Updated
17 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Sponsor
Sanofi

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

1

Lactic Acid (Dermacyd Breeze)

Intervention: Lactic Acid

Outcomes

Primary Outcomes

The absence of primary and accumulated dermical irritability and dermical sensitivity will be evaluated using International Contact Dermatitis Research Group (ICDRG) scale.

Time Frame: Throughout the study

Study Sites (1)

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