Dermal Cryotherapy in Patients Undergoing Abdominoplasty

Status Completed

Clinical Trial Summary

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

Clinical Trial Description

This study is to include healthy adults who intend to undergo an abdominoplasty surgery, and agree to have small areas of their middle and lower abdomen exposed to cooling with the Dermal Cooling System within 180 days before the planned surgery. Exposure of multiple test sites will be completed in areas of skin that will be excised as part of the abdominoplasty procedure. Clinical assessments of the treatment sites at 1-week post-treatment and at 1-month post-treatment intervals throughout the time period prior to surgical excision, and histologic evaluation of the treated skin will be conducted to assess skin changes. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02763306
Study type	Interventional
Source	R2 Dermatology
Contact
Status	Completed
Phase	N/A
Start date	June 2015
Completion date	April 2017

View Details

See also
Status	Clinical Trial	Phase
Active, not recruiting	`NCT06140628` - A 28-day Clinical Study on Facial Skin Rejuvenation	N/A
Completed	`NCT01971736` - Efficacy of Long Pulsed 1064nm Laser for Facial Skin Tightening	N/A
Completed	`NCT01713985` - Feasibility Study: Evaluation of Ulthera Versus Thermage for Treating the Face and Neck	N/A
Completed	`NCT01713998` - Treatment of the Face and Neck With Lower Ulthera System Energy Settings	N/A
Completed	`NCT01708252` - Feasibility Study: Treatment of Post-surgery and Surgery Naive Patients Who Failed to Respond to a Previous Ulthera Treatment	N/A
Completed	`NCT01708382` - Feasibility Study: Lifting and Tightening of the Elbows	N/A
Completed	`NCT04296201` - Evaluation of the Immediate Effect and Safety of DMA™ Novel Muscle Stimulation Technology	N/A
Completed	`NCT06000839` - A Safety and Effectiveness Study of CELLBOOSTER® Lift (Stabilized Booster Complex Using CHAC Technology)	N/A
Completed	`NCT06366503` - Evaluating Procedure Pairing of a Post-Procedure Cream Versus a Comparator in Patients Treated With Fractional Ablative CO2 Laser for Facial Rejuvenation	N/A
Completed	`NCT05929625` - Radiofrequency and Ultrasound for Improvement of Skin Laxity and Wrinkles: Efficacy and Safety Evaluation	N/A
Terminated	`NCT01713569` - Feasibility Study: Histological Characterization After Treatment With the Ulthera® System	N/A
Completed	`NCT01519934` - A Retrospective Study to Evaluate the Effectiveness of the Ulthera System	N/A
Completed	`NCT05605691` - Post-Market Lower Eyelid Treatment With Renuvion in Greece	N/A
Completed	`NCT04477187` - Clinical Assessment of Skin Tightening and Contour Change of Submental Tissue Using Bipolar Radiofrequency Microneedling	N/A
Completed	`NCT05590364` - Aesthetic Performance and Tolerance of an Injective Intradermal Treatment for the Skin Roughness and Laxity of Back of the Hands	N/A
Active, not recruiting	`NCT06243744` - Histological Evaluation of Human Skin Bx to Assess the Effects of APR Tx as an Adjunct Procedure in Facelift Surgery	N/A
Completed	`NCT04146584` - Safety and Efficacy of SofWave Treatment to Lift Lax Tissue in the Submental and Neck Zones and to Lift the Eyebrow	Phase 2
Recruiting	`NCT05750901` - Evaluation of Fractional Ablative Laser Treatment for Skin Conditions	N/A
Completed	`NCT04721600` - Evaluation of the Evoke Radiofrequency Device for Improvement of Skin Appearance	N/A
Recruiting	`NCT06157567` - Clinical Feasibility Study to Evaluate the Safety and Performance of the Profound Matrix System	N/A