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The combination treatment of Botulinum toxin and ablative fractional CO2 lasering to prevent scar formation after thyroidectomy and removal of neck mass

Not Applicable
Conditions
Endocrine, nutritional and metabolic diseases
Registration Number
KCT0006396
Lead Sponsor
The Catholic University of Korea, St. Vincent's Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
75
Inclusion Criteria

Participant who is scheduled to undergo thyroid or tumor in neck through a cervical skin incision, and who heard the explanation of this clinical trial, voluntarily decided to participate and sign it.

Exclusion Criteria

- Children under 19 years old / Seniors over 75 years old
- Pregnant or planning to become pregnant within 6 months, lactating women
- When it is expected that regular follow-up cannot be performed
- No surgery after consent or other surgery (robot surgery or endoscopy)
surgery)
- Myasthenia gravis or peripheral motor nervous system disease
- If had radiation therapy before
- If external radiation is planned after surgery
- If the scheduled operation is a reoperation in the same area
- When a drainage tube is inserted into the skin incision (in case of incision drainage due to deep cervical infection, etc.)
- If known to have keloid
- If allergic to botulinum toxin

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Vancouver scar scale (VSS)
Secondary Outcome Measures
NameTimeMethod
Global assessment score (GAS)
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