Evaluation the effect of a 24 -hour moisturizer

Phase 2

• Conditions: Dry skin.

• Registration Number: IRCT20190210042676N21
• Lead Sponsor: Iran Avandfar Company

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 30 May 2022

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

Male or female aged 18-60 years
The presence of skin dryness
Voluntary participation and signing written informed consent

Exclusion Criteria

Active skin diseases
Active smoking
Pregnancy or breastfeeding
Using systemic corticosteroid in the past 30 days
Use of any topical drugs in the past 7 days
Scar, wound or any condition on the inner forearms that could interfere with a clear-cut assessment of the skin

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The change in stratum corneum hydration after using SynSkin cream. Timepoint: Before intervention and 1 and 4 hours, 24 h, 2weeks after using and one week after not using. Method of measurement: Corneometry.

Secondary Outcome Measures

Name	Time	Method
Trans Epidermal Water Loss. Timepoint: Before intervention and 1 and 4 hours, 24 h, 2weeks after using and one week after not using. Method of measurement: Tewameter.;Skin elasticity. Timepoint: Before intervention and 1 and 4 hours, 24 h, 2weeks after using and one week after not using. Method of measurement: Cutometery.