Clinical trials: Hair Removal
Hypertrichosis
Comparison of Efficacy, Safety and Tolerability of Two Different 810 nm Diode Lasers for Hair Reduction
The purpose of this research study is to compare two different 810 diode laser systems (Soprano XL (SHR Mode)and Light Sheer Duet) for laser hair removal.
- Trial name
- NCT01212172
- Testing
- Soprano/SHR, LightSheer
- Where
- United States
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- University of California, Irvine
Hair Removal
Hair Count Reduction Verification Study With the LightSheer Duet HS Handpiece
The objective of this clinical study is to verify hair count reduction, associated comfort/discomfort and treatment time using the LightSheer Duet System with the High Speed (HS) handpieces for temporary hair removal and…
- Trial name
- NCT01282866
- Testing
- LightSheer Duet
- Where
- United States
- Volunteers
- 35 people, healthy volunteers welcome
- Sponsor
- Lumenis Be Ltd.
Hirsutism
Clinical Evaluation of Silk'n Glide for Face
This is a clinical study to determine the efficacy and safety of the Glide, hair removal photo-depilation device, for removing facial hairs.
- Trial name
- NCT02103608
- Testing
- Glide
- Volunteers
- 17 people, healthy volunteers welcome
- Sponsor
- Home Skinovations Ltd.
Hair Removal
The Efficiency of the Hair2Go Device: A Prospective, Open, Label Study With Before-After Design
The purpose of this study is to determine efficiency of Hair2Go device for short-term and long-term removal of unwanted hair adjunctive to shaving using a before-after study design.
- Trial name
- NCT01348776
- Testing
- Hair2Go (Mē)
- Where
- 4 sites in United States
- Volunteers
- 87 people, healthy volunteers welcome
- Sponsor
- Syneron Medical
Hair Removal
Safety for Frequent Use Conditions of Hair Removal Device
To measure the safety of hair removal device when used frequently.
- Trial name
- OHR-3 (NCT01348789)
- Testing
- Hair2Go (Mē)
- Where
- United States
- Volunteers
- 37 people, healthy volunteers welcome
- Sponsor
- Syneron Medical
Hair Removal
Hair2Go Label Comprehension and Usability Study
The purpose of this study is to test label comprehension and usability of the hair removal device in 60 male and female participants.
- Trial name
- OHR6-LCU (NCT01578187)
- Testing
- Hair2Go
- Where
- United States
- Volunteers
- 63 people, healthy volunteers welcome
- Sponsor
- Syneron Medical
Removal of Excess or Unwanted Body Hair
Clinical Evaluation of Hair Removal and Permanent Hair Reduction for Skin Types VI Using Intense Pulsed Light
This is a Multi-center, blinded, baseline-controlled, prospective study to evaluate permanent hair reduction and removal for skin types V and VI using IPL.
- Trial name
- NCT02452398
- Testing
- Treatment group, No intervention
- Where
- United States
- Volunteers
- 79 people, healthy volunteers welcome
- Sponsor
- Venus Concept
Hair Removal
Ultrasound Device for Hair Removal
The purpose of this study is to evaluate the safety and efficacy of the Cutera UHAIR ultrasound device for hair removal.
- Trial name
- NCT01057134
- Testing
- Cutera Ultrasound Device
- Volunteers
- 10 people, healthy volunteers welcome
- Sponsor
- Cutera Inc.
Pilonidal Disease
Pilot Study of Laser Hair Depilation for Pilonidal Disease
Pilot study to assess tolerability and safety of laser hair depilation in adolescents and young adults with pilonidal disease.
- Trial name
- NCT02778152
- Testing
- Laser depilation
- Where
- United States
- Volunteers
- 13 people
- Sponsor
- Peter Minneci
Hair Removal, Pseudo Folliculitis Barbae
Post Market Study Using The Elite IQ Device
This is a prospective, open label, single-center clinical study to collect safety and efficacy data on the Elite iQ workstation.
- Conditions
- Hair Removal, Pseudo Folliculitis Barbae, Benign Vascular Lesion, Pigmented Lesions
- Trial name
- NCT04807205
- Testing
- RF Non-Invasive Treatment
- Where
- United States
- Volunteers
- 20 people
- Sponsor
- Cynosure, Inc.
Hypertrichosis
Pilot Study of a Novel IPL for Removal of Unwanted Fine Body Hair
The purpose of this randomized, controlled, open-label pilot study is to evaluate the safety and efficacy of a novel intense pulsed light (IPL) device for removal of unwanted fine body hair.
- Trial name
- NCT01912950
- Testing
- Prowave LX IPL
- Where
- United States
- Volunteers
- 11 people, healthy volunteers welcome
- Sponsor
- Cutera Inc.