The combination treatment of Botulinum toxin and ablative fractional CO2 lasering to prevent scar formation after thyroidectomy and removal of neck mass
- Conditions
- Endocrine, nutritional and metabolic diseases
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 75
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.
- 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
Name Time Method Vancouver scar scale (VSS)
- Secondary Outcome Measures
Name Time Method Global assessment score (GAS)