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Mouth Neoplasms clinical trials

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NCT ID: NCT02586207 Active, not recruiting - Clinical trials for Head and Neck Cancer

Pembrolizumab in Combination With CRT for LA-SCCHN

Start date: November 2015
Phase: Phase 1
Study type: Interventional

This is a single-arm, multi-site, open-label trial of pembrolizumab (MK-3475) used in combination with standard, cisplatin-based, definitive chemoradiotherapy (CRT) in patients with stage III-IVB squamous cell carcinoma of the head and neck (SCCHN). Approximately 39 patients with Stage III-IVB SCCHN will be enrolled to evaluate both the safety and efficacy of this novel combination. Subjects will not be randomized and will all receive the study treatment. Treatment will consist of a loading dose of pembrolizumab 200 mg IV given 7 days prior to initiation of CRT (day-7). CRT with cisplatin 40 mg/m2 IV weekly and head and neck radiation at 70 Gy fractionated at 2 Gy once daily over 35 days, will begin on day 1. CRT will end on approximately day 46-50. Pembrolizumab 200 mg IV will continue following CRT in an adjuvant fashion starting on day 57 for an additional 5 doses, as tolerated, through day 141. Subjects will be evaluated for response following treatment.

NCT ID: NCT02584270 Recruiting - Oral Cancer Clinical Trials

Prosthesis Guided Speech Rehabilitation of T1/T2 Cancers of the Tongue

PGSRT
Start date: January 2, 2018
Phase: N/A
Study type: Interventional

This study will fill a scientific gap in the current knowledge providing data for evaluation of the palatal augmentation prosthesis (PAP) as a therapeutic modality in a robust scientific randomized prospective clinical trial. Positive outcomes from this study have the potential to dramatically alter the most common issues of oral cancer therapy, namely speech and swallowing functions. Patients will have been diagnosed with a cancer lesion on their tongue requiring surgery and removal of part of the tongue. Smaller cancers of the tongue are sized as T1 or T2. For patients with smaller lesions, a PAP, which can aid in speaking and swallowing is not routinely provided with the device.

NCT ID: NCT02581137 Active, not recruiting - Oral Leukoplakia Clinical Trials

Metformin Hydrochloride in Preventing Oral Cancer in Patients With an Oral Premalignant Lesion

Start date: June 10, 2016
Phase: Phase 2
Study type: Interventional

This phase IIa trial studies how well metformin hydrochloride works in preventing oral cancer in patients with an oral premalignant lesion (oral leukoplakia or erythroplakia). Oral premalignant lesions look like red or whitish plaques or lesions in the mouth that do not rub off and can be associated with a higher risk of cancer. Metformin hydrochloride may help prevent oral cancer from forming in patients with an oral premalignant lesion.

NCT ID: NCT02507141 Recruiting - Clinical trials for Head and Neck Cancer

Reflectance Confocal Microscopy of Oral Cancers in Vivo: a Preliminary Trial Comparing Intra-oral Imaging With Pathology

Start date: July 21, 2015
Phase:
Study type: Observational

The purpose of this study is to get images (pictures) of oral lesions, which occur inside the mouth, before the patient's surgery using a special camera. These pictures will be used in our research to evaluate a new technology that uses a laser and takes pictures of the microscopic structure of tissue. The technology is called "reflectance confocal microscopy." We would like to compare what the camera sees to biopsies (pathology) of the same area. We will evaluate the pictures obtained from the patient to determine whether this technology may be useful in the future. We hope this technology can be used as a tool for early diagnosis of oral cancers and for guiding surgery.

NCT ID: NCT02478138 Completed - Clinical trials for Head and Neck Neoplasms

Sentinel Lymph Node Mapping of Oral Cancer Using Near-Infrared Fluorescence Imaging

SLN Mapping
Start date: May 2015
Phase: N/A
Study type: Interventional

Cervical lymph node involvement, in head and cancer neck patients, is one of the most important prognostic factors. Currently patients undergo neck dissection removing some or all nodes and neck involvement is retrospectively determined. Sentinel lymph node (SLN) identification and biopsy has become clinical practise in other areas including breast, skin, and gastric cancer. The gold standard for detecting metastatic lymph nodes is pathological analysis, but the lack of an accurate or clinically accepted way to identify sentinel lymph nodes in the cervical region has motivated the usage of indocyanine green (ICG) and near-infrared fluorescence (NIR) imaging (Pinpoint, Novadaq, Waterloo). A prospective clinical trial using a commercially available NIR system and ICG injection around the tumour site will evaluate the ability to detect and biopsy sentinel lymph nodes in head and neck cancer patients.

NCT ID: NCT02412241 Completed - Lymphedema Clinical Trials

Establishing Lymphedema and Fibrosis Measures in Oral Cancer Patients

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

This four-year, prospective, longitudinal study will evaluate and validate a patient-reported outcome measure, clinician-reported outcome measures, and imaging techniques in assessing characteristics, trajectory, and progression of lymphedema and fibrosis (LEF) in oral cavity and oropharyngeal cancer patients. This clinical trial studies patient-and-clinician-reported measures as well as standard imaging methods to see how accurate they are in identifying and evaluating lymphedema (swelling) or fibrosis (tough or tight tissue) in the head and neck region of patients receiving treatment for newly diagnosed stage II-IV oral cavity or oropharyngeal cancer. Lymphedema and fibrosis (LEF) can lead to physical symptoms, such as trouble swallowing and chewing, as well as psychological and emotional symptoms, such as negative body image and avoiding social interactions. Finding an accurate test to identify and evaluate LEF may allow doctors to treat LEF more quickly and control symptoms more effectively, and thus provide patients with a better quality of life.

NCT ID: NCT02323672 Completed - Oral Cancer Clinical Trials

Salivary and Serum Levels of Chemerin and MMP-9 in Oral Premalignant and Malignant Lesions

Start date: February 2014
Phase: N/A
Study type: Observational

45 individuals were subdivided into 3 groups, 15 patients with oral premalignant lesions, 15 patients with oral malignant lesions and 15 control individuals. Levels of chemerin and MMP-9 were evaluated in serum and saliva of these subjects utilizing the ELISA technique.

NCT ID: NCT02290145 Recruiting - Clinical trials for Carcinoma, Squamous Cell

Cyclin D1 Based TPF Induction Chemotherapy for Oral Squamous Cell Carcinoma Patients at Clinical N2 Stage

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

The purpose of this study is to To confirm the predictive value of CCND1 for TPF induction in cN2 patients with OSCC

NCT ID: NCT02285543 Terminated - Clinical trials for Carcinoma, Squamous Cell

A Phase II Trial of TPF Induction Chemotherapy in cN2 OSCC Patients

Start date: December 1, 2016
Phase: Phase 2
Study type: Interventional

To confirm the subgroup result from TPF (docetaxel, cisplatin and 5-fluorouracil ) trial (NCT01542931) that cN2 OSCC patients could benefit from TPF induction chemotherapy compared to the standard treatment.

NCT ID: NCT02285530 Recruiting - Clinical trials for Carcinoma, Squamous Cell

GDF15 Based TPF Induction Chemotherapy for OSCC Patients

Start date: December 1, 2019
Phase: Phase 2
Study type: Interventional

The purpose of this study is to confirm the predictive value of GDF15 expression for TPF induction in T3/T4cN0M0 patients with OSCC