Lactacyd Radiance (Lactic Acid) Prophetic Patch Test

Phase 2CompletedNCT00679562

Sanofi200 enrolled

Overview

Primay objective: To evaluate the potential of the products in eliciting adverse skin reaction.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

200

Conditions

Hygiene

Interventions

Lactic AcidDRUG

Application of occlusive patches containing test product. For 24 hours and repeat 2 weeks later for participants with no reaction to Lactacyd Radiance

Distilled waterOTHER

Application of patches containing distilled water for 24 hours

Eligibility

Sex: ALLMin age: 18 YearsMax age: 60 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Test area should have a healthy or normal skin * Individuals free of any systemic or dermatological disorder which, in the opinion of the investigative personnel would interfere with the study results or increase the risk of adverse reaction * Not currently use of steroid or any medication during the test Exclusion Criteria: * History of Allergy or Allergic Reaction to: * Hey Fever * Asthma * Poison Ivy * Food * Cosmetics * Soap * Detergent * Metal * Jewelry * Lather * Fabric * Medication The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Locations (1)

Sanofi-Aventis Administrative Office

Bangkok, Thailand

Outcomes

Primary Outcomes

Reaction after patch removal.

Time frame: at 15-30 minutes and day 3

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.