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Sponsored by: |
Sanofi-Aventis |
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Information provided by: | Sanofi-Aventis |
ClinicalTrials.gov Identifier: | NCT00785655 |
To demonstrate the absence of irritation potential (primary dermical irritability and cumulated dermical irritability) and allergy (sensibilization) of the product Dermacyd PHDETINLYN Sweet Flower.
Condition | Intervention | Phase |
---|---|---|
Hygiene |
Drug: Dermacyd PH_DETINLYN (Lactic Acid) |
Phase III |
Study Type: | Interventional |
Study Design: | Supportive Care, Non-Randomized, Uncontrolled, Single Group Assignment, Safety/Efficacy Study |
Official Title: | Study for Dermatological Evaluation of Topic Compatibility (Primary and Accumulated Dermical Irritability, Dermical Sensitivity) of Dermacyd PH_DETINLYN (Lactic Acid) Sweet Flower |
Enrollment: | 53 |
Study Start Date: | July 2008 |
Primary Completion Date: | September 2008 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
---|---|
1: Experimental
Dermacyd PH_DETINLYN (Lactic Acid)
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Drug: Dermacyd PH_DETINLYN (Lactic Acid) |
Ages Eligible for Study: | 18 Years to 60 Years |
Genders Eligible for Study: | Female |
Accepts Healthy Volunteers: | Yes |
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.
Responsible Party: | sanofi-aventis ( Medical Affairs Study Director ) |
Study ID Numbers: | LACAC_L_04299 |
Study First Received: | November 4, 2008 |
Last Updated: | November 4, 2008 |
ClinicalTrials.gov Identifier: | NCT00785655 |
Health Authority: | Brazil: National Health Surveillance Agency |