MedPath

Shock wave for treating burn scar

Not Applicable
Conditions
Condition 1: burn scar. Condition 2: burn scar. Condition 3: burn scar. Condition 4: burn scar. Condition 5: burn scar. Condition 6: burn scar.
Burn and corrosion of head and neck
Burn and corrosion of trunk
Burn and corrosion of shoulder and upper limb, except wrist and hand
Burn and corrosion of wrist and hand
Burn and corrosion of hip and lower limb, except ankle and foot
Burn and corrosion of ankle and foot
Registration Number
IRCT2017012132091N1
Lead Sponsor
Isfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
17
Inclusion Criteria

Being older than 18 years with limb burn scar caused by fire
Exclusion criteria: having face, genitalia, thorax and neck scar; being pregnant for women; having coagulopathy and heart pacemaker; Undergoing chemotherapy and radiotherapy; having mental and physical disability; Not cooperating or not referring to continue the treatment

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Burn scar. Timepoint: before the intervention, right after the intervention, 1 month after the end of the intervention, 3 months after the end of the intervention. Method of measurement: Visual Analogue Scale (VAS), Vancouver Scar Scale (VSS), Photographing the scar.
Secondary Outcome Measures
NameTimeMethod
Burning pain. Timepoint: before the intervention, right after the intervention, 1 month after the end of the intervention, 3 months after the end of the intervention. Method of measurement: Viasual Analogue Scale (VAS).;Scar Appearance. Timepoint: before the intervention, right after the intervention, 1 month after the end of the intervention, 3 months after the end of the intervention. Method of measurement: Vancouver Scar Scale (VSS)- photography.;Itching. Timepoint: before the intervention, right after the intervention, 1 month after the end of the intervention, 3 months after the end of the intervention. Method of measurement: Viasual Analogue Scale (VAS).
© Copyright 2025. All Rights Reserved by MedPath