A double blind randomised controlled trial assessing the effect of 30% topical lidocaine gel on reducing pain in patients presenting to a cosmetic surgery practice with either prominent periorbital or lateral temporal veins for treatment with Neodymium-Doped Yttrium Aluminum Garnet (ND:TAG))
Phase 4
Completed
- Conditions
- Surgery - Surgical techniquesPeriorbital and lateral temporal veins - cosmetic
- Registration Number
- ACTRN12613000996763
- Lead Sponsor
- niversity of Toronto
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
1. 18 years of age or older
2. Cosmetically significant lateral temporal or infra-orbital as subjectively judged by the patient
Exclusion Criteria
1. known sensitivity or allergy to any topical or other anaesthetic medication
2. unilateral veins only
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method