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Skin Neoplasms clinical trials

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NCT ID: NCT03754140 Withdrawn - Melanoma Clinical Trials

Intralesional Sclerosant for in Transit and Cutaneous Melanoma Metastases

INTRANS
Start date: May 20, 2020
Phase: Phase 2
Study type: Interventional

There is currently an urgent need for low cost and well tolerated intralesional agents for the management of in transit and cutaneous melanoma metastases that are unsuitable for, or resistant to, other therapies. This pilot study will determine whether intralesional injections of the sclerosant polidocanol into intransit and cutaneous melanoma lesions shows promise for efficacy, safety and ease of use that will enable this inexpensive and widely available agent to undergo further evaluation.

NCT ID: NCT03752736 Completed - Sunburn Clinical Trials

Sun Safety Skills for Elementary School Students

Start date: February 25, 2019
Phase: N/A
Study type: Interventional

The overarching goal of this work is to pilot-test a song-based instructional video designed to help elementary school (kindergarten) age children independently apply sunscreen effectively (i.e., covers all needed areas), efficiently (i.e., can be accomplished in 2-3 minutes), consistently (i.e., continues to apply sunscreen routinely before recess both during and after the intervention), without impacting classroom function (i.e., no mess). The video is also designed to encourage use of hats and sunglasses. The outcomes of interest include identification of "gaps" in skills that are consistent for this age group (i.e., commonly miss application to the back of neck), areas of learning refinement (i.e., generalization of skills with different outfits on), and flexibility in terms of adapting practice (i.e., can they do it without the video). The investigators hope that this pilot project will pave the way for broader clinical / educational implementation of this intervention within schools.

NCT ID: NCT03740815 Completed - Anesthesia Clinical Trials

Feasibility of Serratus Plane Block Associated With Sedation in Axillary Dissection

Start date: September 25, 2018
Phase: N/A
Study type: Interventional

INTRODUCTION: The axillary lymphadenectomy procedure is known to be associated with late postoperative complications, such as chronic pain and changes in shoulder mobility. Recently, several thoracic ultrasound guided interfascial blocks have been described, including serratus plane block. These blocks were associated with reduced postoperative pain scores in breast surgeries but were never evaluated in axillary dissection. The safety and feasibility of performing axillary dissection under local anesthesia and tumescent anesthesia associated with sedation has been demonstrated in case series, although it is not already the standard technique. DISCUSSION: This project aims to investigate the feasibility of the serratus plane block associated with intra-venous sedation in a prospective case series including 15 patients submitted to axillary dissection, by scoring patient and surgeon satisfaction with the technique, pain, quality of life with EORTC QLQ-C30 questionnaire, and quality of recovery with QoR-40 questionnaire in the first 30 postoperative days.

NCT ID: NCT03737734 Active, not recruiting - Skin Cancer Clinical Trials

Alpha Radiation Emitters Device for the Treatment of Cutaneous, Mucosal or Superficial Soft Tissue Neoplasia (DaRT)

Start date: December 31, 2018
Phase: N/A
Study type: Interventional

A unique approach for cancer treatment employing intratumoral diffusing alpha radiation emitter device for superficial cutaneous, mucosal or soft tissue neoplasia

NCT ID: NCT03731247 Completed - Skin Cancer Clinical Trials

Optical Coherence Microscopy in Dermato-oncology

OCTAV
Start date: October 19, 2018
Phase: N/A
Study type: Interventional

OCTAV is a medical device class I, CE marked, based on a new technique for high-resolution imager (cell) internal microstructures of all types of biological tissues in vivo or ex vivo, to a depth of penetration 800 .mu.m. It allows to explore the epidermis, the dermo-epidermal junction and middle dermis in a totally non-invasive (direct contact with the tissue without sampling).

NCT ID: NCT03727789 Terminated - Clinical trials for Clinical Stage IV Cutaneous Melanoma AJCC v8

CBL0137 in Treating Patients With Advanced Extremity Melanoma or Sarcoma

Start date: July 1, 2019
Phase: Phase 1
Study type: Interventional

This phase I trial studies best dose and side effects of CBL0137 in treating patients with extremity melanoma or sarcoma that has spread to other places in the body. Drugs, such as CBL0137, may work by binding to tumor cell deoxyribonucleic acid (DNA) to stop the cell from growing further.

NCT ID: NCT03719131 Active, not recruiting - Clinical trials for Unresectable Melanoma

Rituximab and Hyaluronidase Human in Patients With Advanced Melanoma Undergoing Nivolumab and Ipilimumab Therapy

Start date: June 5, 2019
Phase: Phase 2
Study type: Interventional

This phase II trial studies whether rituximab and hyaluronidase human (Rituxan Hycela) can prevent immune related adverse events in participants with stage III-IV melanoma that cannot be removed by surgery who are undergoing nivolumab and ipilimumab therapy.

NCT ID: NCT03716193 Recruiting - Skin Cancer Clinical Trials

Measurement of the Partial Pressure of Oxygen in Cutaneous Tumors Using Electron Paramagnetic Resonance (EPR) Oximetry

Start date: October 17, 2019
Phase: N/A
Study type: Interventional

This protocol will take measurements of a variety of tumors involving the skin in order to assess changes in tumor oxygen from hyperoxygenation therapy and standard cancer-directed treatments, to demonstrate the clinical feasibility of using in vivo Electron Paramagnetic Resonance (EPR) Oximetry to obtain clinically useful measurements of tumor oxygen levels from cancer patients.

NCT ID: NCT03714828 Completed - Clinical trials for Squamous Cell Carcinoma

Study of TVEC in Patients With Cutaneous Squamous Cell Cancer

Start date: December 20, 2018
Phase: Phase 2
Study type: Interventional

This is single arm a Phase 2, single center study of talimogene laherparepvec (TVEC) to treat low risk cutaneous squamous cell carcinomas (cSCC).

NCT ID: NCT03698019 Active, not recruiting - Clinical trials for Clinical Stage IV Cutaneous Melanoma AJCC v8

A Study to Compare the Administration of Pembrolizumab After Surgery Versus Administration Both Before and After Surgery for High-Risk Melanoma

Start date: February 15, 2019
Phase: Phase 2
Study type: Interventional

This phase II trial studies how pembrolizumab works before and after surgery in treating patients with stage III-IV high-risk melanoma. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving pembrolizumab before and after surgery may work better compared to after surgery alone in treating melanoma.