Clinical Trials Logo

Skin Lesion clinical trials

View clinical trials related to Skin Lesion.

Filter by:

NCT ID: NCT04470466 Completed - Skin Lesion Clinical Trials

Short Pulse and Q-switched ND-YAG Laser With Topical Carbon Versus Fractional CO2 Laser for Enlarged Facial Pores

Start date: July 19, 2020
Phase: N/A
Study type: Interventional

Facial pores are visible topographic features of the skin that reflect openings of pilosebaceous follicles, that may be enlarged causing distress to some individuals. Many patients desire treatment for this condition, which can be an early sign of skin aging. Therapeutic modalities include intense pulsed light, radiofrequency, dermabrasion, oral and topical retinoids, as well as chemical peeling. Lasers, as fractional CO2, short pulse and Q-switched Nd-YAG, can potentially be used in treatment of wide pores. This study aims at the assessment and comparison of therapy with short pulsed and Q-switched Nd-YAG laser plus topical carbon with fractional CO2 laser in the management of wide facial pores.

NCT ID: NCT03914846 Completed - Skin Lesion Clinical Trials

Ultrasound in Diagnosing Patients With Skin Lesions

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

This trial studies the use of a novel non-invasive ultrasound technique in diagnosing patents with skin lesions. Diagnostic procedures, such as ultrasound, may be a less invasive way to check skin lesions for skin cancer and other skin disorders.

NCT ID: NCT03914274 Completed - Skin Lesion Clinical Trials

Adequate Sock to Avoid Hiking Injuries

Start date: October 10, 2015
Phase: N/A
Study type: Interventional

Foot lesions can be developed during hiking because of external factors. This makes it important to study the effect of hiking equipment on lesion development. This study analyzes the extrinsic factors involved in the appearance of injuries at the feet during the realization of a route of low difficulty and short travel. 33 participants wore cotton not technicians socks in his two feet, were used like control socks and 76 participants wore technical socks "Tierra" and "Set" one on each foot.

NCT ID: NCT03612570 Completed - Skin Lesion Clinical Trials

Nano-Pulse Stimulation (NPS) in Sebaceous Hyperplasia

Start date: June 28, 2018
Phase: N/A
Study type: Interventional

This prospective, open label, muti-center study evaluates the use of Nano-Pulse Stimulation (NPS) in the treatment of Sebaceous Hyperplasia (SH) lesions less than 2.5mm in size.

NCT ID: NCT03535077 Completed - Melanoma (Skin) Clinical Trials

Assessing Tissue Remodeling in the Skin Using SFI (Skin Fluorescence Imaging)

Start date: January 24, 2018
Phase:
Study type: Observational

The goal of the SFI is to provide non-invasive information about tissue remodeling occurring during melanocytic transition and atypia development in the skin

NCT ID: NCT03282994 Completed - Skin Lesion Clinical Trials

Dermal Cooling System for Cryotherapy of Common Skin Conditions

Start date: July 19, 2017
Phase: N/A
Study type: Interventional

Prospective, non-randomized, open-label study to evaluate the dermal cooling system for cryotherapy of common skin conditions.

NCT ID: NCT03109327 Completed - Melanoma Clinical Trials

Investigating the Clinical Utility of the MDS

OMS002_UK
Start date: April 1, 2018
Phase:
Study type: Observational

The purpose of this study is to establish the clinical utility of the Melanoma Detection System (MDS).

NCT ID: NCT02740257 Completed - Skin Lesion Clinical Trials

Smartphone Application to Detect Skin Lesions

Start date: March 2016
Phase:
Study type: Observational

The primary objective of Part One of this study is to determine the sensitivity of an automated total body digital photography (TBDP) app to detect color and size changes in the human skin, and whether a new lesion has arisen. The primary objective of Part Two is to test the sensitivity and specificity as well as feasibility of field use of an automated TBDP app to detect pigmented and non-pigmented skin lesions in high risk populations.

NCT ID: NCT02598609 Completed - Clinical trials for Intubation Complication

SEPREVEN: a Stepped-wedge Randomised Controlled Trial

SEPREVEN
Start date: November 23, 2015
Phase: N/A
Study type: Interventional

Adverse events are frequent in Neonatal Intensive Care Units' (NICU) patients and account for a high morbidity and mortality. Possible severe adverse events are central line associated bloodstream infections (CLABSI), ventilator and catheter associated adverse events and medication errors. Severity of the patient's outcome after an adverse event can be classified using the National Coordinating Council for Medication Error Reporting and Preventing (NCC MERP) Index for categorizing medication errors. The study will test the hypothesis that rates of adverse events in NICU patients will be reduced by the implementation of an educational program for the NICU caregivers (nurses and physicians), consisting of strategies for recognizing and preventing adverse events in their unit. These strategies will be oriented to prevent CLABSI, medication errors, skin and nasal complications and ventilator and catheter-associated adverse events. This trial has a stepped wedge cluster design, in which the NICUs from 12 hospitals in France will be randomized to the timing of implementation of the educational program. In order to describe the adverse events occurring during the study period, an anonymous voluntary adverse event reporting system will be provided to the caregivers of the participating units. A nested study will examine how caregivers communicate with the patients' parents in case of adverse event (disclosure or not, and caregivers' reasons). The rates of adverse events will be measured retrospectively using a neonatal NICU trigger tool.

NCT ID: NCT02193581 Completed - Skin Lesion Clinical Trials

Non-invasive Melanoma Assessment Using a Topical Fluorescence Reagent and Optical Imaging

Start date: August 30, 2017
Phase: N/A
Study type: Observational

The use of MDS to access the presence of melanoma in the skin.