Clinical Trials Logo

Skin Neoplasms clinical trials

View clinical trials related to Skin Neoplasms.

Filter by:

NCT ID: NCT02408835 Not yet recruiting - Neoplasm Metastasis Clinical Trials

Negative Pressure Wound Therapy in Groin Dissection

Start date: July 2015
Phase: N/A
Study type: Interventional

This study investigates the use of a negative pressure wound therapy device (PICO™, Smith & Nephew Healthcare, UK) on clean, closed surgical wounds, in patients who are undergoing inguinal lymphadenectomy for metastatic carcinoma of cutaneous origin.

NCT ID: NCT02395562 Completed - Skin Cancer Clinical Trials

Viral Reactivation and Skin Cancer

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

Several studies show that the incidence of skin cancer parallels the length and depth of immunosuppression. This study will analyze the correlation of viral reactivation and skin cancer in organ transplant recipients.

NCT ID: NCT02385214 Active, not recruiting - Clinical trials for Cutaneous Melanoma by AJCC V7 Stage

MelmarT Melanoma Margins Trial Investigating 1cm v 2cm Wide Excision Margins for Primary Cutaneous Melanoma

MelMarT
Start date: January 3, 2015
Phase: Phase 3
Study type: Interventional

Patients with a primary invasive melanoma are recommended to undergo excision of the primary lesion with a wide margin. There is evidence that less radical margins of excision may be just as safe. This is a randomised controlled trial of 1 cm versus 2 cm margin of excision of the primary lesion for adult patients with a primary invasive cutaneous melanomas >=1mm thick to determine differences in the rate of local recurrence and melanoma specific survival. A reduction in margins is expected to improve quality of life in patients

NCT ID: NCT02373722 Completed - Clinical trials for Malignant Skin Neoplasm

Website Application Based Education and Text Messaging in Improving Skin Wound Care in Patients Undergoing Mohs Surgery

Start date: March 2015
Phase: N/A
Study type: Interventional

This randomized clinical trial studies how well website application (web app) based education and text messaging works in improving skin wound care in patients undergoing Mohs surgery (a surgical procedure used to treat skin cancer). Website application and text messaging based education may help patients stick to wound care instructions before and after surgery, lower anxiety level, and may help monitor their activity.

NCT ID: NCT02361229 Active, not recruiting - Skin Cancer Clinical Trials

Skin Cancer in Swiss Transplant Cohort Study

SCSTCS
Start date: January 2008
Phase:
Study type: Observational [Patient Registry]

It's known that organ transplant recipients with long-term drug-induced immunosuppression have a increase of the life-time incidence of squamous cell carcinoma. This study will analyze the incidence and type of skin cancer in the Swiss Transplant Cohort Study and the association with exposure to immunosuppressive and antiinfective drugs and other parameters like age or gender of organ transplant recipients.

NCT ID: NCT02355587 Terminated - Cutaneous Melanoma Clinical Trials

Five Year Study to Track Use of DecisionDX-Melanoma Test in Patients With Cutaneous Melanoma and Associated Patient Outcomes

EXPAND
Start date: March 2014
Phase:
Study type: Observational [Patient Registry]

The EXPAND Registry Study follows patients with cutaneous melanoma who have had the DecisionDx-Melanoma gene expression assay performed as part of their clinical care. Data will be collected through review of medical records from clinical visits with physician. The purpose is to document the clinical application of results obtained from the DecisionDx- Melanoma multi-gene assay and to track outcomes of patients for whom DecisionDx-Melanoma testing has been completed. Additionally the study will assess the health economic impact of DecisionDx-Melanoma testing as it relates to the Melanoma population.

NCT ID: NCT02352428 Active, not recruiting - Melanoma Clinical Trials

Skin Cancer Screening Education Study

SCSES
Start date: February 2015
Phase: N/A
Study type: Interventional

The overall aim of this population-based screening study is to assess whether the skin cancer screening training of family physicians and dermatologists leads to improved screening outcomes. The training course aims to increase the accuracy of detecting early stages of skin cancer. Screening outcomes of an intervention region (Calgary, Canada) in which physicians receive training will be compared with screening outcomes of a control region (Edmonton, Canada) where no physician training is administered. The investigators will determine whether: - clinical screening outcomes are more favorable in the group of trained physicians compared to non trained physicians - there is an increase of knowledge about skin cancer screening among trained physicians, compared to non trained physicians - skin cancer screenings are associated with psycho-social harms - population-based screening has an effect on the overall incidence and stage-specific-incidence of skin cancer in Alberta The investigators are aiming to recruit 100 physicians per region (total of 200 physicians) who will screen 40,000 to 80,000 individuals over a period of 20 months.

NCT ID: NCT02339571 Recruiting - Clinical trials for Stage IV Cutaneous Melanoma AJCC v6 and v7

A Phase II/III Trial of Nivolumab, Ipilimumab, and GM-CSF in Patients With Advanced Melanoma

Start date: November 23, 2015
Phase: Phase 2/Phase 3
Study type: Interventional

This phase II/III trial studies the side effects of nivolumab and ipilimumab when given together with or without sargramostim and to see how well they work in treating patients with stage III-IV melanoma that cannot be removed by surgery (unresectable) and that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). Immunotherapy with monoclonal antibodies, such as ipilimumab and nivolumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Colony-stimulating factors, such as sargramostim, may increase the production of white blood cells. It is not yet known whether nivolumab and ipilimumab are more effective with or without sargramostim in treating patients with melanoma.

NCT ID: NCT02324608 Completed - Clinical trials for Squamous Cell Carcinoma of the Skin

Cetuximab Before Surgery in Treating Patients With Aggressive Locally Advanced Skin Cancer

Start date: January 30, 2015
Phase: N/A
Study type: Interventional

This pilot clinical trial studies the side effects and how well cetuximab before surgery works in treating patients with skin cancer that forms, grows, and spreads quickly and has spread from where it started to nearby tissue or lymph nodes. Monoclonal antibodies, such as cetuximab, may block tumor growth in different ways be targeting certain cells. Giving cetuximab before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed.

NCT ID: NCT02321982 Withdrawn - Clinical trials for Basal Cell Carcinoma

Same-day Versus Separate-day Preoperative Consultation for Mohs Surgery

Start date: February 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether separate- versus same-day preoperative consultation affects time to treatment (start to finish), utilization rate of Mohs, rate of case cancellations, cost, and patient satisfaction. The investigators hypothesize that patients with same-day preoperative consultation will have a shorter time between cancer diagnosis and removal but, only when coordination of care is needed, longer time between removal and consultation with other specialists, as compared to patients with separate-day consultation. The investigators anticipate that patients with same-day preoperative consultation will have a decrease in travel cost as compared to patients with separate-day consultation. The investigators expect that there will be no difference in various satisfaction matters between groups, with the exception of potentially greater convenience reported by patients in the same-day preoperative consultation group. Finally, the investigators hypothesize that there will be no difference between groups in regards to rates of surgery cancellation.