Clinical Trials Directory

Trials / Completed

CompletedNCT01305057

Efficacy Test on Skin Hydration and Skin Barrier Function

Human Use Test on Skin Hydration and Skin Barrier Function

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Cosmos Technical Center · Industry
Sex
All
Age
33 Years – 62 Years
Healthy volunteers
Accepted

Summary

The effects of topically applied pyridoxine tri-isopalmitate (P-IP) which stimulates filaggrin synthesis in keratinocytes, on skin hydration and barrier function were examined. Subjects were separated into two groups to examine the effect of P-IP. Subjects were treated with P-IP formulation on one side of the face and with a placebo formulation on the other side twice daily (morning and evening) for 28 days. All subjects gave written informed consent prior to the study. The skin hydration and TEWL (transepidermal water loss) were evaluated by measuring skin surface conductance with a skin hygrometer SKICON 200EX (I.B.S. ltd., Japan) and TEWL meter AS-CT1 (ASAHI BIOMED, Tokyo, Japan), respectively.

Detailed description

It is expected that the long-term application of P-IP increase skin surface water contents and suppress TEWL.

Conditions

Interventions

TypeNameDescription
OTHERPyridoxine tri-isopalmitate2% dosage, oil-in-water emulsion, twice a day, 28 days

Timeline

Start date
2009-02-01
Primary completion
2009-02-01
Completion
2009-02-01
First posted
2011-02-28
Last updated
2011-02-28

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT01305057. Inclusion in this directory is not an endorsement.