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
| Type | Name | Description |
|---|---|---|
| OTHER | Pyridoxine tri-isopalmitate | 2% 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.