Topic Compatibility Lactoserum (Dermacyd Delicata - New Fragrance)

Dermatological Evaluation of Topic Compatibility (Primary and Accumulated Dermical Irritability and Dermical Sensitivity) for Dermacyd Femina Delicata

Status

Completed

Phases

Phase 4

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00497692

Enrollment

Registered

2007-07-09

Start date

2007-05-31

Completion date

Unknown

Last updated

2008-05-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hygiene

Brief summary

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.

Interventions

DRUGLactoserum

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

SUPPORTIVE_CARE

Masking

NONE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 60 Years

Healthy volunteers

Yes

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.

Design outcomes

Primary

Measure	Time frame
Score evaluation of the cutaneous reaction, preconized by International Contact Dermatitis Research Group (ICDRG)	six weeks

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026