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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02396290
Other study ID # 2012-0998
Secondary ID
Status Completed
Phase N/A
First received March 9, 2015
Last updated March 17, 2015
Start date March 2013
Est. completion date September 2013

Study information

Verified date July 2013
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Investigation of Clinical Effect of Platelet Rich Plasma Combined With Laser on Acne Scar


Description:

Platelet Rich Plasma may relieve the adverse effect of laser treatment. and it can be expected to improve acne treatment result.


Recruitment information / eligibility

Status Completed
Enrollment 29
Est. completion date September 2013
Est. primary completion date September 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 19 Years to 40 Years
Eligibility Inclusion Criteria:

- moderate to severe acne scar

Exclusion Criteria:

- taken procedures for acne scar within 6 months

- underlying diabetes mellitus, keloid, or malignancy

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
fractional carbon dioxide laser with platelet rich plasma
fractional carbon dioxide laser followed by platelet rich plasma injection
fractional carbon dioxide laser with NS
fractional carbon dioxide laser followed by normal saline injection

Locations

Country Name City State
Korea, Republic of Department of Dermatology, Seoul National University College of Medicine Seoul

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

References & Publications (1)

Tierney EP, Eisen RF, Hanke CW. Fractionated CO2 laser skin rejuvenation. Dermatol Ther. 2011 Jan-Feb;24(1):41-53. doi: 10.1111/j.1529-8019.2010.01377.x. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Global assessment of acne scar 5-point grading of acne scar 12 weeks No
Secondary ECCA (échelle d'évaluation clinique des cicatrices d'acné) quantitative analysis of acne scar 12 weeks No
Secondary adverse effect assessment adverse effect assessment - erythema index, Epithelization Scale (0-12 point) 12 weeks Yes
See also
  Status Clinical Trial Phase
Recruiting NCT04648995 - TheTreatment of Acne Scar Using UltraPulse CO2 Laser N/A
Completed NCT05573425 - Comparing the Efficacy of Topical Tazarotene Gel 0.1% v/s Microneedling in Atrophic Post Acne Scars Phase 2/Phase 3