Lactacyd Radiance (Lactic Acid) Prophetic Patch Test

Primay objective:

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

Completed

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Key information

Conditions

Hygiene

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Sanofi-Aventis Administrative Office

Bangkok, Thailand

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Lactic acid

Drug

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

Other names: Lactacyd Radiance

Distilled water

Other

Application of patches containing distilled water for 24 hours

Primary outcomes

Reaction after patch removal.

Time frame: at 15-30 minutes and day 3

Sponsors and collaborators

Lead sponsor

Sanofi

Industry

Registry information

Official study title

Skin Irritation : Prophetic Patch Test of Lactacyd Radiance

Important dates

Study start: 2008
Primary completion: 2008
First posted: May 19, 2008
Registry last updated: Feb 6, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed