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Acceptability Dermacyd Delicata - New Fragrance - Lactoserum - Hygiene

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00370162
First Posted: August 30, 2006
Last Update Posted: May 16, 2008
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Sanofi
August 29, 2006
August 30, 2006
May 16, 2008
June 2006
Not Provided
Adverse Events and its association with the drug in study
Same as current
Complete list of historical versions of study NCT00370162 on ClinicalTrials.gov Archive Site
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Acceptability Dermacyd Delicata - New Fragrance - Lactoserum - Hygiene
Safety Dermatological Evaluation: Acceptability With Gynecological Follow up - Dermacyd Delicata New Fragrance
The purpose of this study is to demonstrate the safety of the gynaecological formulation in normal and usual usage condition.
Not Provided
Interventional
Phase 3
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Hygiene
Drug: lactoserum
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Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
30
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Inclusion Criteria:

  • Integral skin in the tested region

Exclusion Criteria:

  • Pregnancy or breastfeeding women
  • Use of antiinflammatory or immunosuppression drugs
  • Topical medication use at the tested region
  • Active cutaneous gynaecological disease
  • Personal history of allergic disease at the area to be treated
  • Allergic or atopic history
Sexes Eligible for Study: Female
18 Years to 60 Years   (Adult)
Yes
Contact information is only displayed when the study is recruiting subjects
Brazil
 
 
NCT00370162
LACTO_L_01839
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Sanofi
Not Provided
Study Director: Jaderson Lima Sanofi
Sanofi
May 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP