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Nevus clinical trials

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NCT ID: NCT01324609 Terminated - Nevus Clinical Trials

Detection of Choroidal Nevus Cells in Vitrectomy Fluid

Start date: June 2010
Phase:
Study type: Observational

The purpose of this study is to determine if the investigators can detect the presence of choroidal nevi cells in the vitreous fluid of humans, as this may improve the diagnosis and classification of choroidal nevi and melanomas in the future.

NCT ID: NCT01194947 Not yet recruiting - Clinical trials for Common Melanocytic Nevi

Classification and Longitudinal Follow-up of Common Melanocytic Nevi With in Vivo Reflectance Confocal Microscopy

Start date: September 2010
Phase: N/A
Study type: Observational

Our working hypothesis is that reflectance confocal microscopy (RCM) can identify distinct subsets of melanocytic nevi that retain their distinctive pattern over time.

NCT ID: NCT01167998 Active, not recruiting - Malignant Melanoma Clinical Trials

Early Diagnosis of Malignant Transformation of Pigmentary Skin Lesions

Start date: July 2010
Phase:
Study type: Observational

Malignant Melanoma is a deadly skin cancer that can be cured if diagnosed early. To date atypical pigmented skin lesions are diagnosed by appearance alone and many moles and lesions are excised unnecessarily and on the other hand malignant lesions are missed and diagnosed too late. In this study a protein conjugated to a florescent dye is spread on a suspicious pigmented lesion, the hypothesis is that this protein binds to malignant cells only and thus with a special camera that picks up the dye we can find pigmented lesions with early malignant transformation.

NCT ID: NCT00957229 Completed - Clinical trials for Basal Cell Nevus Syndrome

To Determine The Efficacy and Safety of GDC-0449 in Patients With Basal Cell Nevus Syndrome (BCNS)

GDC-0449
Start date: August 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to reduce the number of new surgically eligible BCCs by 50% appearing during month 3-18 of medication ingestion.

NCT ID: NCT00955578 Not yet recruiting - Clinical trials for Segmental Dysplastic Nevi

Genetic Identification (ID) of Segmental Dysplastic Nevi

Start date: August 2009
Phase: N/A
Study type: Observational

The investigators' goal is to identify the mutation in the gene that is responsible for the development of segmental dysplastic nevi. To identify the gene the investigators may use a candidate gene approach (i.e. sequence specific genes that are thought to be involved: NRAS, BRAF, etc) or a genome-wide approach trying to implicate regions in the genome (Loss-of-heterozygosity or copy number changes on comparative genomic hybridization).

NCT ID: NCT00656227 Active, not recruiting - Cicatrix Clinical Trials

A Trial to Investigate Scar Improvement Efficacy of RN1001 (Avotermin) After Head and Neck Naevi Excision

Start date: April 2004
Phase: Phase 2
Study type: Interventional

This trial will investigate whether four doses of RN1001 (20ng, 50ng, 100ng and 200ng) are efficacious in preventing or reducing the resultant scar, as compared to placebo, when applied intradermally to wound margins following excision of benign naevi situated on the head and neck.

NCT ID: NCT00600431 Completed - Nevus, Pigmented Clinical Trials

Melanocytic Nevi in Children Under Chemotherapy

Start date: February 2006
Phase: N/A
Study type: Observational

Changes in nevus count in 16 children (8m, 8f) aged between 2 and 17 years (median:8 years) suffering from different malignancies were examined every three months during a one-year period after starting chemotherapy. An age and sex matched control group underwent the same skin examinations.At the start of our study, the range of number of nevi in the chemotherapy group was 0-133, in the control group 2-199.

NCT ID: NCT00487864 Completed - Nevus Clinical Trials

In Vivo Confocal Scanning Laser Microscopy of Benign Nevi

CSLM-nevi
Start date: September 2006
Phase: N/A
Study type: Observational

In vivo confocal laser scanning microscopy (CLSM) offers the possibility to non-invasively investigate skin lesions at nearly histologic resolution. A recent study showed a high sensitivity (97.6%) and specificity (88.15%) for the discrimination of clinical clear cut melanocytic lesions. CSLM provides horizontal images and can be seen as missing link between dermoscopy and histopathology. For a more accurate diagnosis of dermoscopically difficult to diagnose melanocytic skin lesions in the grey zone between nevus and melanoma, the knowledge of CLSM features of benign nevi seems to be essential. We investigated 30 flat benign nevi with different dermoscopic patterns (10 reticular, 10 globular, 10 homogeneous) nevi. CLSM images were assessed in terms of cytomorphologic and architectural criteria. Different dermoscopic patterns of benign nevi are reflected in different architectural features in CLSM.

NCT ID: NCT00422448 Completed - Nevi Clinical Trials

Study to Test Genetic Alterations Among Different Dermoscopic Types of Melanocytic Nevi.

Start date: September 2006
Phase: N/A
Study type: Interventional

This project is a multicenter study in which we will investigate a dual concept of nevogenesis. Study location is the Department of Dermatology at the Medical University of Graz in collaboration with centers in Austria (Vienna), Italy (Naples, Benevento, Modena), Spain (Barcelona) and the United States (New York). The hypothesis is that small congenital melanocytic nevi (CMN), "early" acquired melanocytic nevi in childhood (AMN) and dermal nevi, all dermatoscopically characterized by globular pattern, belong to the same spectrum of genetically determined melanocytic proliferations that develop due to endogenous pathways, in contrast to "true" acquired melanocytic nevi, dermatoscopically showing reticular pattern, that develop due to exogeneous factors such as UV-exposure.

NCT ID: NCT00346502 Withdrawn - Clinical trials for Dysplastic Nevus Syndrome

Evaluation of 20% Betulinic Acid Ointment for Treatment of Dysplastic Nevi (Moderate to Severe Dysplasia)

Start date: January 2006
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of an experimental 20% betulinic acid ointment (BA ointment) as a treatment for dysplastic nevi with the potential to transform into melanoma.