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Dermacyd Infantile - Acceptability.

Safety Dermatological Evaluation: Acceptability With Paediatric Follow up Dermacyd Infantile (Lactic Acid).

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00881270
Enrollment
31
Registered
2009-04-15
Start date
2009-03-31
Completion date
2009-03-31
Last updated
2009-09-28

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 prove the safety of the formulation in normal conditions of use.

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
No minimum to 12 Years
Healthy volunteers
Yes

Inclusion criteria

* Integral skin test in the region * Use the same category of cosmetics * Willingness in following the study procedures and to be present in the clinic at the days and scheduled time.

Exclusion criteria

* Use of Anti-inflammatory, immunosuppressant or anti-histaminic drugs * Allergic or atopic history to cosmetics products * Cutaneous active disease (local or general) in the evaluated area * Disease which can cause immunosuppressant, such as diabetes, HIV * Endocrine pathology * Intensive solar exposure until 15 days before evaluation * Treatment four months before selection. 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 absence of irritation and the good acceptability will be evaluated using one specific scale which describes the intensity of the reaction.From the treatment start to the end of the study

Countries

Brazil

Outcome results

None listed

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