Evaluation of VeinViewer in Cosmetic Dermatology
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 75
- Locations
- 4
- Primary Endpoint
- Patient perception of the use of the device
Study Overview
Brief Summary
This study aims to understand the impact of VeinViewer technology during routine cosmetic and dermatologic procedures.
Detailed Description
This study was designed as an observational study to determine if VeinViewer technology helped to improve the efficiency of certain dermatological procedures namely botox injections and schlerotherapy for varicose veins. The device was used to identify veins but clinical decisions were ultimately left the physician.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Supportive Care
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •18 years of age and up
- •Male or Female
- •Receiving cosmetic dermatological injection
- •Willing to participate
Exclusion Criteria
- •Aged younger than 18 years
- •Prior history of known light sensitivity
- •Other reasons as determined by investigator
Arms & Interventions
VeinViewer
VeinViewer will be used in conjunction with routine cosmetic dermatology procedures. Patients and physicians will complete questionnaires.
Intervention: VeinViewer (Device)
Outcomes
Primary Outcomes
Patient perception of the use of the device
Time Frame: Day 1
Small questionnaires will be used to assess how the patient perceives the use of the device (i.e., did the patient have a positive attitude towards the device?)
Secondary Outcomes
- Physician perception of the use of the device(Day 1)