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Skin Neoplasms clinical trials

View clinical trials related to Skin Neoplasms.

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NCT ID: NCT04221438 Active, not recruiting - Clinical trials for Pathologic Stage IIIC Cutaneous Melanoma AJCC v8

Testing Treatment With Encorafenib and Binimetinib Before Surgery for Melanoma With Lymph Node Involvement

Start date: September 22, 2021
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well encorafenib and binimetinib work before surgery in treating patients with BRAF V600-mutated stage IIIB-D melanoma that has spread to the lymph nodes. Encorafenib and binimetinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. This trial also studies how well 18F-FLT positron emission tomography (PET)/computed tomography (CT) works in predicting the response of melanoma to encorafenib and binimetinib. 18F-FLT is an imaging agent, sometimes called a tracer. PET and CT are types of imaging scans. Using 18F-FLT PET/CT together with encorafenib and binimetinib may provide more information on melanoma over time.

NCT ID: NCT04206995 Completed - Skin Cancer Clinical Trials

Cancer Sensing: Evaluation of Odour Sampling Techniques

Start date: September 1, 2021
Phase:
Study type: Observational

To evaluate the suitability of two odour capturing techniques for early detection of skin cancer.

NCT ID: NCT04204837 Recruiting - Clinical trials for Squamous Cell Carcinoma of the Skin

Nivolumab for Treatment of Squamous Cell Carcinoma of the Skin

Start date: March 6, 2017
Phase: Phase 2
Study type: Interventional

To determine the Objective Response Rate (ORR) of immunotherapy with Nivolumab (Group 1) and Nivolumab plus Relatlimab (Group 2) in patients with locally advanced/metastatic squamous cell carcinoma of the skin using Response Criteria in Solid Tumors Version 1.1 (RECIST1.1) per site assessment (Time Frame Group 2: From first dose up to 5 years)

NCT ID: NCT04176900 Withdrawn - Skin Cancer Clinical Trials

3D Printed Rigid Bolus Versus Silicone Bolus for Treatment of Tumors Involving the Skin: A Comparative Study

Start date: March 2020
Phase: N/A
Study type: Interventional

This study compares two types of 3D-printed skin bolus (rigid and flexible) used to optimize the treatment of tumors/cancers involving the skin. Each patient will have both types of bolus made, with each will be used on alternating days. The goal is to determine if one type of bolus provides a better fit and thus radiotherapy plan, the ease of use of each type of bolus, and patient reported feedback.

NCT ID: NCT04176237 Completed - Skin Neoplasm Clinical Trials

School-based Randomized Trial of SunSmart Interventions

Start date: January 1, 2014
Phase: N/A
Study type: Interventional

The objective of this study is to test a novel classroom-based intervention to motivate youth to limit their sun exposure. The intervention will make the process of learning about sun exposure more person-centered using individual dosimetry readings and feedback that will lead to individual plans for reducing sun exposure.

NCT ID: NCT04164550 Completed - Clinical trials for Skin Cancer, Non-Melanoma

Interpolated Flap Study

Start date: April 18, 2018
Phase:
Study type: Observational

The primary purpose of this study is to address the limited knowledge regarding patient well- being and nasal function after interpolated flap repair of post-Mohs surgical defects on the nose. Improved understanding of the patient experience will allow providers to better counsel their patients pre-operatively and potentially identify patients who may benefit from additional interventions.

NCT ID: NCT04163419 Active, not recruiting - Pain Clinical Trials

Phase 2 Study of Tanezumab in Subjects With Moderate to Severe Pain Due to Schwannomatosis

Start date: April 30, 2020
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to determine whether the administration of tanezumab, an anti-nerve growth factor (NGF) antibody, improves pain relief in schwannomatosis patients receiving background non-NSAID therapy.

NCT ID: NCT04160065 Active, not recruiting - Clinical trials for Merkel Cell Carcinoma

Immunotherapy With IFx-Hu2.0 Vaccine for Advanced Non-melanoma Skin Cancers

Start date: March 3, 2020
Phase: Phase 1
Study type: Interventional

In this clinical phase I, non-randomized, open-label, uncontrolled, interventional, multi-center trial, 20 adult subjects (≥ 18 years of age) with advanced non-melanoma skin cancers will receive a fixed dose of 0.1 mg of IFx-Hu2.0 intralesionally as monotherapy in up to three lesions at up to three time points. Subjects will be observed for any acute adverse events (AEs) post injection and for any delayed AEs at Day 28, 35 and/or 42 ± 7 days, depending on the cohort (exposure escalation and expansion design).

NCT ID: NCT04138342 Recruiting - Breast Cancer Clinical Trials

Topical Fluorescent Nanoparticles Conjugated Somatostatin Analog for Suppression and Bioimaging Breast Cancer

Start date: September 15, 2019
Phase: Phase 1
Study type: Interventional

Breast cancer is a communal malignant disease between Saudi females, with a popularity of 21.8%. Since binding to somatostatin receptors (SSTR) induces no immunogenicity in vivo, somatostatin analog (veldoreotide) (VELD) may be suitable for delivering anti-cancer drugs to target and bioimaging the cancer cells. This work aimed to deliver CdS/ZnS core-shell type quantum dots with carboxylic acid-functionalized (QDs-COOH) which is bioimaging and anticancer nanoparticles decorated VELD as SSTR agonist with anti-cancer activity in the form of topical cream to be deposited deep in the breast periphery.

NCT ID: NCT04127318 Withdrawn - Immunotherapy Clinical Trials

Low-moderate Intensity Pedaling During Immunotherapy Administration

Start date: January 31, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the feasibility pedaling using an under-the desk bike during immunotherapy infusions. Also, the study hopes to evaluate how pedaling impacts quality of life and treatment response biomarkers. Lastly, the study will evaluate the relationships between treatment response and muscle mass which is evaluated with computerized tomography (CT) scans.