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Dermacyd Infantile (Lactic Acid) - Photo Evaluation.

Dermatological Evaluation of the Photo Irritation and Photo Sensitivity Potential for Dermacyd Infantile (Lactic Acid).

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00881348
Enrollment
25
Registered
2009-04-15
Start date
2009-02-28
Completion date
2009-03-31
Last updated
2009-04-15

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

Conditions

Hygiene

Brief summary

Primary Objective: To demonstrate the absence of photo irritation and photosensitization potential of the product Dermacyd Infantile (Lactic Acid).

Interventions

Dermacyd infantile (Lactic Acid)

Sponsors

Sanofi
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Phototype Skin I, II, III and 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 Anti-inflammatory, immunosuppressant or anti-histaminic drugs * Lactation or gestation * Use of Anti-inflammatory drugs 30 days and/or immunosuppressant drugs during 3 months before the selection * Diseases which can cause immunity decrease, such as HIV, diabetes * Previous atopy * History of sensitivity or irritation for topic products * Active cutaneous diseases which can interfere in the study results * Use of new drugs and/ or cosmetics during the study * Cutaneous reactivity * Previous participation in studies, which had used the product * Volunteers who have immunodeficiency congenital or acquired. The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Design outcomes

Primary

MeasureTime frame
The photo irritation test and the photosensitivity will be measured using UVA irradiation and evaluated according International Contact Dermatitis Research Group (ICDRG) scale. The sensibility will be evaluated according to the skin type.During 5 weeks (i.e. treatment period)

Countries

Brazil

Outcome results

None listed

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