ClinicalTrials.Veeva

Menu

Efficacy Test on Skin Hydration and Skin Barrier Function

C

Cosmos Technical Center

Status

Completed

Conditions

Dry Skin

Treatments

Other: Pyridoxine tri-isopalmitate

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT01305057
hydration-1 (Other Identifier)
Cosmos1

Details and patient eligibility

About

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.

Full description

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

Enrollment

20 patients

Sex

All

Ages

33 to 62 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • healthy skin

Exclusion criteria

  • don't use any moisturizer

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

20 participants in 1 patient group

Evaluation of P-IP on hydration and barrier function
Experimental group
Description:
Effects of P-IP on improvement of skin hydration and TEWL were examined.
Treatment:
Other: Pyridoxine tri-isopalmitate

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems