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Laser System
GentleMax Pro Plus 755nm and 1064nm laser system for Hirsutism
N/A
Waitlist Available
Research Sponsored by Candela Corporation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Presence of unwanted hair of desired characteristics and treatment location to be evaluated in this study
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months
Awards & highlights
Study Summary
This trialstudies laser hair removal to permanently reduce fine facial hair with a device called GentleMax Pro Plus™.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
You cannot have the specific type of hair in the treatment area that we are studying.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Improvement in hair removal/ hair clearance
Incidence, severity, and relatedness of adverse events
Secondary outcome measures
Laser Hair Removal improvement
Subject satisfaction with treatment results
Other outcome measures
Subject Pain Assessment
Trial Design
1Treatment groups
Experimental Treatment
Group I: Unwanted Fine Facial HairExperimental Treatment1 Intervention
Up to three (3) treatments with GentleMax Pro/ GentleMax Pro Plus TM for Laser Hair Removal
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Who is running the clinical trial?
Candela CorporationLead Sponsor
19 Previous Clinical Trials
1,945 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I agree to not have any other procedures, medications, or topicals done in the areas where the study is taking place for the duration of the study.The patient is willing to allow pictures and videos of the treated area, and agrees to the use of these images for scientific or educational purposes, as well as for promotional or marketing purposes.is essential to prevent resurgence of the infectionYou cannot have the specific type of hair in the treatment area that we are studying.
Research Study Groups:
This trial has the following groups:- Group 1: Unwanted Fine Facial Hair
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Who else is applying?
What state do they live in?
New York
How old are they?
18 - 65
What portion of applicants met pre-screening criteria?
Did not meet criteria
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