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Skin Laxity clinical trials

View clinical trials related to Skin Laxity.

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NCT ID: NCT04176068 Completed - Skin Laxity Clinical Trials

Combined Focused Ultrasound and Calcium Hydroxylapatitie Filler for Skin Laxity and Volume Restoration

Start date: April 19, 2019
Phase: Phase 1
Study type: Interventional

Non-invasive treatment options such as focused ultrasound has been used with success for the treatment of skin laxity in various parts of the body including the face, neck, décolletage, arms, buttocks, thighs, and legs. With the increasing demand for greater results, researchers have started combining modalities together such as focused ultrasound and intradermal filler, with promising effects for skin laxity and volume restoration. This study aims to elucidate the efficacy and added benefits of a combination therapy using focused ultrasound (Ulthera) and calcium hydroxylapatite (Radiesse) for the treatment of skin laxity and volume restoration of the lower thighs, specifically the lower anterior third of the thigh.

NCT ID: NCT04146584 Completed - Wrinkle Clinical Trials

Safety and Efficacy of SofWave Treatment to Lift Lax Tissue in the Submental and Neck Zones and to Lift the Eyebrow

Start date: November 20, 2019
Phase: Phase 2
Study type: Interventional

This is a prospective, open label, multi-center, self-controlled clinical study to demonstrate the safety and efficacy of SofWave treatment to lift lax tissue in the submental and neck zones and to lift the eyebrow.

NCT ID: NCT03969485 Completed - Skin Laxity Clinical Trials

Hybrid Fractional Laser for Treatment of Off Face Body Skin Quality

Start date: April 29, 2019
Phase: N/A
Study type: Interventional

To demonstrate effectiveness of hybrid fractional laser for the treatment of poor skin quality on the decolletage, back of the hands and lower legs

NCT ID: NCT03966924 Completed - Lipodystrophy Clinical Trials

The PREFORM Study: Rotational Fractional Resection for Submental Contouring

Start date: March 20, 2019
Phase: N/A
Study type: Interventional

This study will evaluate the safety and efficacy of rotational fractional resection (RFR) to improve neck contouring. Rotational fractional resection is used to remove loose skin and fat.

NCT ID: NCT03534609 Completed - Wrinkle Clinical Trials

Lutronic Genius System for Neck Treatment

Start date: March 27, 2018
Phase: N/A
Study type: Interventional

The Genius system is substantially equivalent to the Infini device (K121481). The study is a prospective, multi-site, non-randomized study of up to 30 treated subjects presenting for treatment of mild to moderate lines, wrinkles, textural concerns, and/or skin laxity of the neck.

NCT ID: NCT03507036 Completed - Skin Laxity Clinical Trials

Radio Frequency Microneedling for Suprapatellar Skin

Start date: March 15, 2018
Phase: N/A
Study type: Interventional

The human skin aging process is characterized by thinning dermis, atrophy of the extracellular matrix, and reduced collagen synthesis. Loss of collagen in the dermis is of aesthetic concern, as it is the main structural support in the dermis and its loss results in skin laxity. Photo-damaged skin, mostly due to UVR, causes degradation of elastic fibers. This is histologically seen as disorganized tangles of elastin. Additionally, as humans age, skin tends to appear more dry due to its poor hydration and turgor capacity. The use of minimally invasive aesthetic treatments in reducing signs of aging has been gaining in popularity over surgical treatments in recent years. Several energy types including, laser, radiofrequency, infrared, and ultrasound, have been developed for facial rejuvenation. These treatments induce controlled thermal damage into the dermis and cause collagen contraction and neocollagenesis resulting in skin tightening over several months. For improving appearance of other anatomical areas, micro-focused ultrasound has been the preferred method, but has shown limited success in tightening the suprapatellar skin. As with facial skin aging, the suprapatellar skin loses elasticity with age and begins to sag. Noninvasive treatments used for the face may also be used in other anatomical areas to produce the same effects of tightening. Minimally invasive bipolar radiofrequency produces a controlled thermal injury in a fractional manner without damaging the dermal-epidermal junction, epidermis or subcutis. Radiofrequency, unlike lasers, are chromophore-independent providing better penetration than lasers, and spare sweat glands, sebaceous glands, and hair follicles.

NCT ID: NCT03407313 Completed - Lipodystrophy Clinical Trials

CONFORM: Rotational Fractional Resection for Submental Contouring

Start date: January 8, 2018
Phase: N/A
Study type: Interventional

This study will evaluate the safety and efficacy of rotational fractional resection (RFR) to improve neck contouring. RFR is used to remove loose skin and fat.

NCT ID: NCT02832674 Completed - Skin Laxity Clinical Trials

Safety and Effectiveness Evaluation of the Device in Achieving Submental Lift

Start date: June 25, 2016
Phase: N/A
Study type: Interventional

A prospective evaluation of the ThermiRF device in treating skin laxity under the chin and neck. Seventy male and female subjects between the age of 35 and 65 (inclusive) will be enrolled in this trial. The first 30 subjects will have a total of 6 study visits while the remainder will have a total of 5 study visits. All subjects will have a single treatment administered. The first 30 subjects will have an extra visit at Day 60 intended to allow collection of photo images post treatment to be used for the validation of three blinded raters. Photo images will be collected using 2D standard photography and 3D using the Vectra system. The architecture of the skin in the affected area will be measured using the Cutometer, a suction like instrument that measures elasticity. Sensory and safety will be measured using a 0-10 point numerical rating scale (NRS) and collection of safety reports. The study duration is approximately 6 months.

NCT ID: NCT02770287 Completed - Skin Laxity Clinical Trials

Radiofrequency and Pulsed Electromagnetic Field Treatment of Skin Laxity of the Mon Pubis, Labia and Vaginal Introitus

Start date: March 26, 2016
Phase: N/A
Study type: Interventional

The study will confirm that the Freeze Diamond polar applicator is safe for treating the Mons pubis and Labia, and will result in improvement in general skin appearance including an improvement in skin irregularities and skin laxity.

NCT ID: NCT02763306 Completed - Skin Laxity Clinical Trials

Dermal Cryotherapy in Patients Undergoing Abdominoplasty

Start date: June 2015
Phase: N/A
Study type: Interventional

A prospective, interventional, single-arm study to evaluate histologic changes in skin following cryotherapy with the study device.