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Cutis Laxa clinical trials

View clinical trials related to Cutis Laxa.

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NCT ID: NCT03599349 Completed - Clinical trials for Facial and Neck Skin Laxity

Evaluation of the Ulthera® System and Efficacy Correlation to Morphological Differences

Start date: August 20, 2015
Phase: N/A
Study type: Interventional

Evaluate if there is a correlation between efficacy results and where the Thermal Coagulation Points (TCPs) produced during a treatment with the Ulthera System make contact with anatomical layers of the skin and underlying tissues.

NCT ID: NCT03583918 Completed - Laxity; Skin Clinical Trials

Efficacy of Micro-excisional Skin Removal by Micro-coring Device in Treatment of Wrinkles and Laxity of Face and Neck

MCD
Start date: June 1, 2017
Phase: N/A
Study type: Interventional

This is a prospective, multi-center, pilot study evaluating effectiveness of micro-excisional skin remodeling by micro-coring skin in subjects meeting the Inclusion Criteria. Subjects will undergo bilateral treatment on the face and neck (upper and lower cheek, upper and lower lip, periocular and perioral areas, submandibular and middle neck, etc). The exact treatment area(s), choice of treatment density are left to the Investigator's discretion and subject's consent. Up to 3 treatments are allowed with a minimum of 30-day between the consecutive treatments.

NCT ID: NCT03573271 Recruiting - Laxity; Skin Clinical Trials

Pivotal Study to Evaluate the Effectiveness of a Micro-coring Device Treating Moderate to Severe Facial Wrinkles

Start date: March 22, 2018
Phase: N/A
Study type: Interventional

Study evaluating the effectiveness of a micro-coring device for the treatment of moderate to severe cheek wrinkles.

NCT ID: NCT03545412 Completed - Facial Skin Laxity Clinical Trials

Clinical Study on the Application of a Non-Invasive Micro-Focused Ultrasound With Visualization System for Skin Laxity (ULT-215)

ULT-215
Start date: January 10, 2014
Phase: N/A
Study type: Interventional

To evaluate the effect of the Ulthera® system for facial laxity and sagging skin

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: NCT03487172 Completed - Knee Clinical Trials

Sculptra Aesthetic for the Treatment of Upper Knee Skin Laxity

Start date: April 10, 2018
Phase: N/A
Study type: Interventional

All subjects will receive three, single-sided injections of PLLA, performed 1 month apart.

NCT ID: NCT03440697 Recruiting - Clinical trials for Aortic Valve Disease

Pathogenetic Basis of Aortopathy and Aortic Valve Disease

TAA
Start date: December 10, 2015
Phase:
Study type: Observational

The main purpose of this study is to define the complex genetic and pathogenic basis of thoracic aortic aneurysm (TAA) and other forms of aortopathy and/or aortic valve disease by identifying novel disease-causing genes and by identifying important genetic modifiers for aortic and aortic valve disease severity.

NCT ID: NCT03351335 Completed - Clinical trials for Mild to Moderate Skin Laxity Under the Chin

Open-label, Prospective Evaluation of the Ulthera® System for Lifting Submental (Under the Chin) and Neck Tissue in Chinese Patients

ULT-302
Start date: August 10, 2017
Phase: N/A
Study type: Interventional

To evaluate the Ulthera® System for lifting submental (under the chin) and neck tissue in Chinese patients

NCT ID: NCT03280069 Recruiting - Clinical trials for Meibomian Gland Dysfunction

Evaluation of Ocular Surface Changes Following RF Electrocoagulation Treatment of the Periorbital Region

Start date: July 25, 2017
Phase: N/A
Study type: Observational

This protocol will evaluate THERMIeyes® for its ability to treat periorbital skin laxity and wrinkles and monitor ocular surface changes and their effect on evaporative dry eye associated with MGD.