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Topic Compatibility Lactoserum (Dermacyd Delicata - New Fragrance)

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Sanofi

Status and phase

Completed
Phase 4

Conditions

Hygiene

Treatments

Drug: Lactoserum

Study type

Interventional

Funder types

Industry

Identifiers

NCT00497692
LACTO_L_02948

Details and patient eligibility

About

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 Femina Delicata.

Enrollment

30 estimated patients

Sex

Female

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Phototypes: I, II, III and IV
  • Integral skin test in the region

Exclusion criteria

  • Pregnancy or breastfeeding women
  • Use of antinflammatory or immune-suppression drugs
  • Personal history of atopy
  • History of sensibilization or irritation for topic products
  • Active cutaneous disease
  • Use of new drugs and/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.

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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