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Clinical Trials/NCT04187586
NCT04187586CompletedNot Applicable

Effect of Extracorporeal Shock Wave Therapy for Burn Scar Charateristics: A Retrospective Study

Hangang Sacred Heart Hospital1 site in 1 country35 target enrollmentStarted: December 10, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
35
Locations
1
Primary Endpoint
scar thickness

Study Overview

Brief Summary

No study has investigated the effect of extracorporeal shock wave therapy (ESWT) on hypertrophic scar characteristics. Thus, this study aimed to ascertain the effects ESWT on burn scars. The investigators retrospectively reviewed burn patients who had undergone autologous split-thickness skin grafting (STSG) with same artificial dermis between January 2012 and September 2019.

Detailed Description

No study has investigated the effect of extracorporeal shock wave therapy (ESWT) on hypertrophic scar characteristics. Thus, this study aimed to ascertain the effects ESWT on burn scars. The investigators retrospectively reviewed burn patients who had undergone autologous split-thickness skin grafting (STSG) with same artificial dermis between January 2012 and September 2019. The ESWT group (n=17) received shock waves with low-energy flux density (0.05-0.30 mJ/mm2). The interval between treatments is a 1-week. The ESWT group also received standard treatment. The control group (n=18) only received standard treatment. We reviewed skin characteristics before and after 6 treatment sessions for both groups. The investigators checked skin charateristics(erythema, transepidermal water loss, sebum level, and elasticity). The investigators expect that ESWT is effective for significantly improving burn-associated scar characteristics and may be used for managing burn patients.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • a retrospective review of 35 patients who had undergone STSG between January 2012 and September 2019
  • limited to the upper extremities(the upper arm, forearm, and hand)
  • the scars which undergone STSG with same artificial dermis using Matriderm® (MeSkin Solution Dr. Suwelack AG, Billerbeck, Germany)

Exclusion Criteria

  • not evaluated serial assessments
  • below 18 years age

Outcomes

Primary Outcomes

scar thickness

Time Frame: 6 weeks

hypertrophic scar thickness check using ultrasonic wave equipment (128 BW1 Medison, Korea).

Secondary Outcomes

  • scar transepidermal water loss(TEWL)(6 weeks)
  • scar erythema(6 weeks)
  • Sebum(6 weeks)
  • Elasticity(6 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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