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Nevus clinical trials

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NCT ID: NCT02809001 Completed - Scar Clinical Trials

The Effects of Autologous Fat Transfer on Preventing Expanded Skin From Expansion Failure

Start date: January 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate whether autologous fat grafting is safe and/or effective to prevent expanded skin from expansion failure.

NCT ID: NCT02722798 Completed - Clinical trials for Tumor-Induced Osteomalacia or Epidermal Nevus Syndrome

A Study of KRN23 in Subjects With Tumor-Induced Osteomalacia or Epidermal Nevus Syndrome

Start date: April 2016
Phase: Phase 2
Study type: Interventional

Before switching to the post-marketing study: To evaluate the efficacy and safety of KRN23 after its 144-week once every 4 weeks (Q4W) repeated SC administration to Japanese and Korean patients with TIO or ENS by a multicenter, open-label, intraindividual dose adjustment study. After switching to the post-marketing study: To evaluate the safety and efficacy of KRN23, which is switched from the investigational product to the post-marketing investigational product, at the approved dose and dosing regimen in subjects who continue treatment after the marketing approval of KRN23 in Japan.

NCT ID: NCT02354261 Completed - Clinical trials for Basal Cell Carcinoma in Basal Cell Nevus Syndrome

Open-label Trial of SUBA™-Itraconazole (SUBA-Cap) in Subjects With Basal Cell Carcinoma Nevus Syndrome (BCCNS)

Start date: August 7, 2015
Phase: Phase 2
Study type: Interventional

The study will assess the safety and efficacy of SUBA-Cap in subjects with Basal Cell Carcinoma Nevus Syndrome.

NCT ID: NCT02304367 Completed - Clinical trials for Tumor Induced Osteomalacia (TIO)

Study of Burosumab (KRN23) in Adults With Tumor-Induced Osteomalacia (TIO) or Epidermal Nevus Syndrome (ENS)

Start date: March 24, 2015
Phase: Phase 2
Study type: Interventional

The primary objectives of this study are to evaluate the effect of burosumab treatment on: - Increasing serum phosphorus levels in adults with TIO or ENS-associated osteomalacia - Improvement in TIO/ENS-associated osteomalacia as determined by osteoid thickness (O.Th), osteoid surface/bone surface (OS/BS), osteoid volume/bone volume (OV/BV) and mineralization lag time (MLt).

NCT ID: NCT02157623 Completed - Clinical trials for Basal Cell Nevus Syndrome

Blue vs Red Light During Levulan Based Photodynamic Therapy in Patients With Basal Cell Nevus Syndrome

Start date: February 1, 2016
Phase: N/A
Study type: Interventional

The investigators will be testing whether aminolevulinate-based (Levulan™) Photodynamic Therapy (PDT) shows effectiveness in the treatment and prevention of cutaneous basal cell carcinoma (BCC) in Basal Cell Nevus Syndrome (BCNS) patients. Levulan™ PDT is an FDA-approved method widely used currently for squamous precancers of the skin. The investigators hypothesize that PDT will provide exceptional benefit in the BCNS population because PDT is nonmutagenic, nonscarring, and can be safely repeated many times. Additionally, the study will investigate whether there are any differences in tumor clearance between the Blu-U® (blue lamp) and Aktilite™(red lamp) therapies.

NCT ID: NCT02100371 Completed - Clinical trials for Basal Cell Nevus Syndrome

Study of BMS-833923 in Two Specific Patients With Basal Cell Nevus Syndrome

Start date: February 2014
Phase: N/A
Study type: Interventional

This is an extension study of Protocol CA194002 to allow 2 specific participants with basal cell nevus syndrome in the CA194002 study at Princess Margaret Cancer Centre who are still benefitting from the study drug BMS-833923 to continue receiving the study drug. This study will continue to evaluate the safety and tolerability of BMS-833923 in these participants.

NCT ID: NCT02012751 Completed - Melanoma Clinical Trials

Nevus Doctor Clinical Decision Support

Start date: October 2014
Phase: N/A
Study type: Interventional

The "Nevus doctor" is a dermatoscopy based computer decision support tool to assist general practitioners (GPs) in the classification of pigmented skin lesions (PSLs). The aim of the program "Nevus doctor" is to help GPs increase their diagnostic accuracy, in particular regarding the selection of suspicious PSLs that need biopsy or referral to specialist health care for further assessment. The aim of this study is to investigate the diagnostic performance of the decision support tool in a primary care setting in Norway. We hypothesize that the diagnostic accuracy of the computer program "Nevus doctor" is better than the performance of the GPs.

NCT ID: NCT01968681 Completed - Nevus Flammeus Clinical Trials

Treatment of Nevus Flammeus With Alexandrite Laser

Start date: September 2013
Phase: N/A
Study type: Interventional

Nevus flammeus is a congenital vascular malformation. Nevus flammeus is traditionally treated with pulsed dye lasers (PDL); however, around 20 percent of patients are poor responders and do not get satisfactory results from pulsed dye laser treatments. Small studies with alexandrite lasers indicate that this may be an alternative treatment for individuals with nevus flammeus. This study assesses the clinical effect and side effects of alexandrite laser treatment for nevus flammeus using different treatment settings.

NCT ID: NCT01568996 Completed - Melanoma Clinical Trials

Pilot Study Evaluating Sulforaphane in Atypical Nevi-Precursor Lesions

Start date: August 2012
Phase: Early Phase 1
Study type: Interventional

This is a pilot study to see if oral administration of freeze dried, powdered broccoli sprouts have any effect on whether moles end up becoming melanoma.

NCT ID: NCT01444560 Completed - Cutaneous Melanoma Clinical Trials

miRNA Machinery in Melanoma, Melanoma Metastases and Benign Melanocytic Naevi

Start date: December 2008
Phase: N/A
Study type: Observational

MicroRNAs (miRNAs) are very small endogenous RNA molecules about 22-25 nucleotides in length, capable of post-transcriptional gene regulation. miRNAs bind to their target messenger RNAs (mRNAs), leading to cleavage or suppression of target mRNA translation based on the degree of complementarity. miRNAs have recently been shown to play pivotal roles in diverse developmental and cellular processes and linked to a variety of skin diseases and cancers. In the present study, the investigators examines the expression profiles of miRNA machinery components such as miRNA maturation and transport factors, microprocessor complex and RISC subunits in cutaneous melanoma, cutaneous melanoma metastases and benign melanocytic nevi.