Dermatological Evaluation of Topic Compatibility-Dermacyd Tina Gel Tangerina Mix
This study has been completed.
Information provided by:
First received: April 23, 2008
Last updated: January 27, 2009
Last verified: January 2009
The purpose of this study is to demonstrate the absence of irritation potential (primary dermic irritability and cumulated dermic irritability) and allergy (sensibilization) of the product Dermacyd Tina Gel Tangerina Mix
Drug: Lactic acid (Dermacid)
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Supportive Care
||Study for Dermatological Evaluation of Topic Compatibility (Primary and Accumulated Dermical Irritability, Dermical Sensitivity) of Dermacyd Tina Gel Tangerina Mix.
Primary Outcome Measures:
- The absence of primary and accumulated dermal irritability and dermal sensitivity will be evaluated using International Contact Dermatitis Research Group (ICDRG) scale. [ Time Frame: six weeks ] [ Designated as safety issue: Yes ]
| Study Start Date:
| Primary Completion Date:
||January 2008 (Final data collection date for primary outcome measure)
|Ages Eligible for Study:
||18 Years to 60 Years
|Genders Eligible for Study:
|Accepts Healthy Volunteers:
- Phototype Skin I,II, III e IV
- Integral skin test in the region
- Lactation or gestation
- Use of Antiinflammatory and/or immunosuppression drugs
- Personnel history of atopy
- History of sensitivity or irritation for topic products
- Active cutaneous disease
- Use of new drugs or cosmetics during the study
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00669058
|Sanofi-aventis administrative office
|São Paulo, Brazil |
||Sanofi-aventis administrative office Brazil
No publications provided
||GMA-CO/Medical Director, sanofi-aventis administrative office France
History of Changes
|Other Study ID Numbers:
|Study First Received:
||April 23, 2008
||January 27, 2009
||Brazil: National Health Surveillance Agency
Keywords provided by Sanofi:
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on October 29, 2014