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CompletedNCT00679562

Lactacyd Radiance (Lactic Acid) Prophetic Patch Test

Skin Irritation : Prophetic Patch Test of Lactacyd Radiance

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
200 (actual)
Sponsor
Sanofi · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

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

Conditions

Interventions

TypeNameDescription
DRUGLactic AcidApplication of occlusive patches containing test product. For 24 hours and repeat 2 weeks later for participants with no reaction to Lactacyd Radiance
OTHERDistilled waterApplication of patches containing distilled water for 24 hours

Timeline

Start date
2008-03-01
Primary completion
2008-04-01
First posted
2008-05-19
Last updated
2009-02-06

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT00679562. Inclusion in this directory is not an endorsement.

Lactacyd Radiance (Lactic Acid) Prophetic Patch Test (NCT00679562) · Clinical Trials Directory