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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01742247
Other study ID # PNUHDM-laser and moisturizers
Secondary ID
Status Completed
Phase Phase 4
First received December 3, 2012
Last updated March 29, 2016
Start date September 2012
Est. completion date December 2015

Study information

Verified date March 2016
Source Pusan National University Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Assessment of needs of moisturizers after various laser treatments


Description:

The investigators would like to assess of needs of moisturizers after various laser treatment

: by investigating the changes in the skin barrier function after fractional carbon dioxide laser and fractional Er:Glass laser in mice and human skin


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date December 2015
Est. primary completion date April 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- at least 18 years of age without any dermatologic diseases

Exclusion Criteria:

- Taking other known dermatologic disease

- Others who are shown pigmented lesion on treated-area

- Who have allergy or history of hypersensitivity reaction to moisturizers

- Who have other definitive cutaneous findings

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Other:
Physiogel
Application of moisturizer on laser-treated area
Moisturizer
Application of moisturizer on laser-treated area

Locations

Country Name City State
Korea, Republic of Department of dermatology, Pusan National University Hospital Busan

Sponsors (1)

Lead Sponsor Collaborator
Pusan National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical assessment of erythema, transepidermal water loss The clinical assessment of erythema, pigmentation, transepidermal water loss will be evaluated by using apparatus. 2weeks No
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