Dermacyd Femina (Lactic Acid) Pocket BR - Photo Evaluation
NCT ID: NCT00783640
Last Updated: 2008-12-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE3
27 participants
INTERVENTIONAL
2008-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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1
Lactic Acid
Lactic Acid
Drug: Lactic Acid (Dermacyd Femina)
Interventions
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Lactic Acid
Drug: Lactic Acid (Dermacyd Femina)
Eligibility Criteria
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Inclusion Criteria
* Phototype Skin I,II, III e IV
* Integral skin test in the region;
* Willingness in following the study procedures and to be present in the clinic at the days and scheduled time for medical evaluations and for application of occlusion;
Exclusion Criteria
* Use of Antiinflammatory and/or immunosuppression drugs one month before the study;
* Personnel history of atopy;
* History of sensitivity or irritation for topic products;
* Active cutaneous disease;
* Use of new drugs or cosmetics during the study;
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
18 Years
60 Years
FEMALE
Yes
Sponsors
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Sanofi
INDUSTRY
Responsible Party
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sanofi-aventis
Principal Investigators
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Jaderson Lima
Role: STUDY_DIRECTOR
Sanofi
Locations
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Sanofi-Aventis Administrative Office
São Paulo, , Brazil
Countries
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Related Links
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Related Info
Other Identifiers
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LACAC_L_04371
Identifier Type: -
Identifier Source: org_study_id