Silk'n HST for Wrinkle Reduction - Clinical Study Protocol

Status Completed

Clinical Trial Summary

The objective of the study is to evaluate the safety, efficacy and usage compliance of the home-use device Silk'n HST for self-treatment of periorbital wrinkles and skin laxity and improvement of skin appearance.

Clinical Trial Description

This is a single arm prospective study of 18 weeks aimed to evaluate the safety and efficiency of Silk'n HST treatment on the periorbital areas. 30 subjects will be enrolled by a single USA clinical site. Throughout the trial there will be 3 pre-scheduled face to face treatment visits, as well as additional 18 independent treatments at home. 2 additional follow-up visits will be conducted 1 and 3 months following treatment end. In addition, 2 maintenance treatment will be conducted independently at home once a month following treatment end. ;

Study Design

Related Conditions & MeSH terms

Wrinkles

Clinical Trial Details

NCT number	NCT02913547
Study type	Interventional
Source	Home Skinovations Ltd.
Contact
Status	Completed
Phase	N/A
Start date	November 2015
Completion date	June 2016

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT01984619` - Prospective Study Evaluating the Treatment of Hyperdynamic Forehead Wrinkles	N/A
Completed	`NCT01713985` - Feasibility Study: Evaluation of Ulthera Versus Thermage for Treating the Face and Neck	N/A
Recruiting	`NCT01586819` - Lateral Canthal Rhytides With Medium Depth Chemical Peel With or Without Pretreatment With Botulinum Toxin A	Phase 3
Completed	`NCT05254210` - Feasibility Study To Collect Safety And Preliminary Efficacy Data For A Radiofrequency Microneedling Device	N/A
Completed	`NCT02604641` - Assessment of the Impact of a Coenzyme Q10 Supplementation on the Skin	N/A
Completed	`NCT01460927` - TriActive+ Radiofrequency (RF) for Non-invasive Treatment of Wrinkles & Rhytides	N/A
Completed	`NCT01519934` - A Retrospective Study to Evaluate the Effectiveness of the Ulthera System	N/A
Completed	`NCT03811756` - The Effect of 12-week Dietary Intake of Syrup Containing CoQ10 and Collagen on Dermis Density and Other Skin Parameters	N/A
Completed	`NCT04988412` - The Effect of 12-week Dietary Intake of Food Supplements Containing Collagen on Dermis Density and Other Skin Parameters	N/A
Active, not recruiting	`NCT02019004` - A Pilot Study Testing Onabotulinum Toxin A Versus Incobotulinum Toxin A Injections for Facial Wrinkles	N/A
Completed	`NCT02340078` - A Clinical Study to Evaluate the Efficacy and Safety of YVOIRE Volume Plus Versus YVOIRE Volume in Nasolabial Fold Injection	N/A
Completed	`NCT01283464` - Comparison of Retinol 1.0% and Tretinoin 0.02% in the Treatment of Moderate to Severe Photodamage and Wrinkles	Phase 2
Completed	`NCT01034956` - Outcomes and Patient Experience After Soft Tissue Dermal Filler Injections	N/A
Completed	`NCT02425943` - Sculptra Aesthetic Post-Approval Study	Phase 4
Recruiting	`NCT05847530` - Pilot Evaluation of the Cynosure Potenza™ System for Treatment of Cosmetic Dermatologic Skin Conditions	N/A
Enrolling by invitation	`NCT01847066` - Epidermal Delivery of Ani-Aging Ingredients	N/A
Completed	`NCT01859611` - TriActive+ Radiofrequency (RF) for Non-Invasive Treatment of Wrinkles and Rhytides	N/A
Completed	`NCT01297634` - Radial Diffusion of the Botulinum Toxin Type A (Botox®): Electromyographic Evaluation of the Frontal Muscle	Phase 4
Completed	`NCT05011461` - The Effect of Topical Almond Oil vs. Topical Retinol on The Appearance of Facial Wrinkles	N/A
Completed	`NCT03460860` - Astaxanthin (2 mg) + Lycopene (1.8 mg) + D-Alpha-Tocopherol (10 IU) For The Treatment Of Skin Aging	N/A