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Cutis Laxa clinical trials

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NCT ID: NCT04795622 Completed - Clinical trials for Improvement in Skin Laxity of the Lower Face and Submentum

Evaluation of the Effectiveness and Safety of the Ulthera® DeepSEE® System for Treating Skin Laxity in the Lower Face and Submentum

Start date: March 16, 2021
Phase: N/A
Study type: Interventional

1. Demonstrate superiority of treatment with the Ulthera DeepSEE System compared to untreated control for the improvement of skin laxity of the lower face and submental area. 2. Demonstrate the safety of treatment with the Ulthera DeepSEE System for the improvement of skin laxity of the lower face and submental area.

NCT ID: NCT04721600 Completed - Skin Laxity Clinical Trials

Evaluation of the Evoke Radiofrequency Device for Improvement of Skin Appearance

Start date: November 1, 2020
Phase: N/A
Study type: Interventional

Evaluation of the Evoke Radiofrequency Device for Improvement of Skin Appearance

NCT ID: NCT04719013 Completed - Laxity; Skin Clinical Trials

Treatment With the Evoke System for Facial and Submental Laxity

Start date: December 1, 2020
Phase: N/A
Study type: Interventional

The aim of the study is to evaluate the efficacy, patient comfort, and patient satisfaction after Evoke treatment for face and submental area

NCT ID: NCT04585217 Completed - Ptosis, Eyelid Clinical Trials

A Comparison of the Effect of Suture Material on Blepharoplasty Incision

Start date: May 30, 2020
Phase: N/A
Study type: Interventional

The objective is to compare the effect of suture material on blepharoplasty incision. Outcomes of blepharoplasty scar and/or cosmesis will be compared between plain gut and polypropylene suture. Additionally, the study will assess whether certain Fitzpatrick skin types are associated with increased rates of poor outcomes after blepharoplasty.

NCT ID: NCT04477187 Completed - Skin Laxity Clinical Trials

Clinical Assessment of Skin Tightening and Contour Change of Submental Tissue Using Bipolar Radiofrequency Microneedling

Start date: October 1, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of bipolar fractional radiofrequency treatment via use of the Profound System to achieve skin tightening and contour change in lax submental (beneath the chin) tissue.

NCT ID: NCT04390581 Completed - Skin Laxity Clinical Trials

A Study to Evaluate the Effect of Juvederm Volift With Lidocaine on Aging Hands in Participants Age 35 and Older

Start date: May 20, 2020
Phase: Phase 4
Study type: Interventional

This study will evaluate the effect of Juvederm Volift with Lidocaine, an injectable gel implant, to treat aging hands of participants 35 and older.

NCT ID: NCT04249128 Completed - Skin Aging Clinical Trials

Nourishing Hair, Skin & Nails Supplement Study (Derm Aid)

Start date: January 15, 2020
Phase: Phase 3
Study type: Interventional

A 90 day eight arm virtual interventional study looking at the impact of various supplement formulations for improves in hair, skin & nail health via self report, and dermatology assessment via remote dermatologist assessment.

NCT ID: NCT04239768 Completed - Face Skin Laxity Clinical Trials

Efficacy of an Antiage Aesthetic Treatment for the Middle and Inferior Third of the Face

Start date: October 14, 2019
Phase: N/A
Study type: Interventional

Primary endpoint of the study is to evaluate clinically and by non-invasive instrumental evaluations the aesthetic performance, on the third middle and inferior of the face, of "MonoDermà HA Bio-revitalizing gel", an intradermal filler containing hyaluronic acid, combined to a low level laser therapy (LLLT) to obtain a stable photo-cross-linking effect inside the dermis.

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.