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Mouth Neoplasms clinical trials

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NCT ID: NCT03082534 Active, not recruiting - Clinical trials for Head and Neck Cancer

Pembrolizumab Combined With Cetuximab for Treatment of Recurrent/Metastatic Head & Neck Squamous Cell Carcinoma

Start date: March 28, 2017
Phase: Phase 2
Study type: Interventional

This is a prospective, multi-center, open-label, non-randomized, multi-arm phase II trial to evaluate the efficacy of combination therapy with pembrolizumab and cetuximab for patients with recurrent/metastatic HNSCC. There will be four patient cohorts, including a PD-1/PD-L1 inhibitor-naïve, cetuximab-naïve arm (Cohort 1), a PD-1/PD-L1 inhibitor-refractory, cetuximab-naïve arm (Cohort 2), a PD-1/PD-L1 inhibitor-refractory, cetuximab-refractory arm (Cohort 3), and a cutaneous HNSCC arm (Cohort 4). A total of 83 patients (33 in Cohort 1, 25 in Cohort 2, 15 in Cohort 3, and 10 in Cohort 4) will be eligible to enroll. Patients will be enrolled at 4 sites: UC San Diego Moores Cancer Center, UC Los Angeles Jonsson Comprehensive Cancer Center, University of Michigan Comprehensive Cancer Center, and University of Washington Siteman Cancer Center.

NCT ID: NCT03067610 Completed - Clinical trials for Head and Neck Cancer

Involved Field Elective Volume De-Intensification Radiation Therapy for Head and Neck Cancer

INFIELD
Start date: January 20, 2017
Phase: Phase 2
Study type: Interventional

Intensity modulated radiation therapy (IMRT) with or without chemotherapy (if given, either cisplatin, cetuximab, or carboplatin-paclitaxel)

NCT ID: NCT03021993 Completed - Oral Cavity SCC Clinical Trials

Trial of Nivolumab as a Novel Neoadjuvant Pre-Surgical Therapy for Locally Advanced Oral Cavity Cancer

Start date: May 30, 2017
Phase: Phase 2
Study type: Interventional

The purpose of this study is to look at the effectiveness of nivolumab in patients with oral cavity cancer (OCC) who are about to undergo surgery.

NCT ID: NCT03017053 Recruiting - Oral Cancer Clinical Trials

The Optimal Neck Treatments Strategy of Early Oral Cancer Based on Adverse Pathological Factor

Start date: July 2016
Phase: Phase 4
Study type: Interventional

Cervical nodal metastasis is the most certain prognostic factor in oral cancer. Appropriate management of the neck is therefore of paramount importance in the treatment of oral cancer. However, there is still some controversy on the treatment of early maxillofacial malignancies. Currently, investigators have no accurate uniform treatment standards, including the National Comprehensive Cancer Network (NCCN) recommended between surgery and radiotherapy options. Clinical evaluation indicated that lymph node-negative patients eventually 25%-35% had cervical node metastasis. Therefore, for the majority of patients with true node-negative, preventive cervical lymph node dissection is obviously over-treatment, and lower quality of life. Radiotherapy can avoid such surgery.

NCT ID: NCT03010813 Completed - Clinical trials for Colorectal Neoplasms

A Novel Robotic System for Single Port and Natural Orifice Transluminal Endoscopic Surgery

Start date: December 2016
Phase: N/A
Study type: Interventional

This is a prospective, single center, multispecialty study that aimed to evaluate the clinical feasibility and safety of single port surgery and NOTES (mainly transanal and transoral surgery) using a novel single port robotic system.

NCT ID: NCT03008694 Not yet recruiting - Oral Cancer Clinical Trials

Effect of FDG-PET/CT for Simulation and Radiation Treatment Planning in Oral Cancer Patients

Start date: January 2017
Phase: Phase 2
Study type: Interventional

This study evaluates the effect of FDG-PET/CT for Simulation and Radiation Treatment Planning in oral Cancer patients. Progress-free survival (PFS) will be compared with historical control as defined in the protocol

NCT ID: NCT02981862 Completed - Cervical Cancer Clinical Trials

CaptHPV : Validation of the Method "CaptHPV" for the Diagnosis of Human Papillomavirus Associated Infiltrating Carcinomas

CaptHPV
Start date: December 19, 2016
Phase: N/A
Study type: Interventional

The current project is based on the assumption that a diagnosis of human papillomavirus associated Infiltrating Carcinomas can be made from a blood sample for patient with Cervical Cancer, Vulvar Cancer, Anal Cancer, Oropharynx Cancer, Oral Cavity Cancer or Penis Cancer at any stage of the disease and including surgical treatment for the small tumors.

NCT ID: NCT02960724 Recruiting - Neoplasms Clinical Trials

uPAR PET/CT for Staging Advanced and Localised Oral and Oropharyngeal Cancer

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

uPAR PET/CT for Staging Advanced and Localised oral and oropharyngeal cancer

NCT ID: NCT02946671 Completed - Lung Cancer Clinical Trials

Study of Pre-operative Combination Therapy With Mogamulizumab and Nivolumab Against Solid Cancer Patients

Start date: March 2016
Phase: Phase 1
Study type: Interventional

To assess the safety of preoperative combination therapy with KW-0761 (anti-CCR4) and ONO-4538 (anti-PD-1). To assess the behavior of immune cells in peripheral blood and tumor.

NCT ID: NCT02923258 Completed - Clinical trials for Oral Cavity Squamous Cell Carcinoma

Postoperative CCRT With Docetaxel vs Cisplatin in High Risk Oral Cavity Cancer

Start date: April 21, 2018
Phase: Phase 2/Phase 3
Study type: Interventional

This is a randomized,controled, phase II, open label study of postoperative concurrent chemoradiotherapy with Docetaxel versus Cisplatin for high-risk squamous cell carcinoma of the oral cavity cancer.The primary purpose of this study is to evaluate the efficacy of concurrent chemoradiotherapy with docetaxel in OCC patients.