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Lip Neoplasms clinical trials

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NCT ID: NCT01424358 Completed - Oral Cancer Clinical Trials

Web-based Education on Oral Cancer for Primary Care Physicians in Ohio

Start date: July 2011
Phase: N/A
Study type: Interventional

Objective: The experimental design is a one-site, randomized experimental web-based educational feasibility intervention trial, with approximately 50% primary care physicians (PCPs) in the intervention group and approximately 50% PCPs on the control group, giving a total of 159 participants. All 159 participants have willingly provided their e-mail addresses, as part of a survey they previously completed entitled, "Survey of Health Professionals on Oral Cancer in Ohio- Intervention to Prevent Delayed Diagnosis of Oral Cancer."

NCT ID: NCT01351532 Completed - Oral Cancer Clinical Trials

Behavior Change on Oral Cancer Patients After a Localized Behavior Change Model Intervention

Start date: April 2011
Phase: N/A
Study type: Interventional

The purpose of this research is to apply this smoking cessation program on oral cancer patients, and to analyze the effectiveness of it.

NCT ID: NCT01136265 Active, not recruiting - Oral Cancer Clinical Trials

PET/CT and Sentinel Node in Oral Cancer

PETNode
Start date: June 2010
Phase: N/A
Study type: Observational

In this study, the investigators want to pre-operatively scan patients who do not have any clinically suspicion of metastases with an 18F-FDG-PET/CT whole body scan , where after they go to lymphoscintigraphy incl. SPECT/CT and sentinel node biopsy. Material from the oral cancer and, after permission of each patient, also normal oral tissue will be analyzed molecular-biologically. Also a blood sample will be analyzed for molecular tumor markers. The investigators want to see if PET/CT is able to detect any signs of sub-clinically metastases. Besides, the investigators want to fusion PET/CT with SPECT/CT data from the lymphoscintigraphy study and improve our PET/CT scanning with a dual-time PET scan of the head-and-neck region.

NCT ID: NCT01084733 Completed - Clinical trials for Oropharyngeal Cancer

Nicotine Levels With Response Rates to Radiation Alone or With Chemo In Head & Neck Cancer

Start date: August 2007
Phase:
Study type: Observational

The objective of this study is to evaluate the relationship between serum nicotine levels and tumor response of squamous cell cancers of the head and neck (SCCHN) to radiotherapy alone or in combination with chemotherapy. Correlation of RECIST response, volumatic response, pathologic response (in patients receiving post-treatment neck dissection), and hemodynamic response (tumor oxygenation and blood flow) will be performed.

NCT ID: NCT00750503 Completed - Oral Cancer Clinical Trials

Workplace Tobacco Cessation And Oral Cancer Screening Study

Start date: June 2007
Phase: Phase 3
Study type: Interventional

Tata Memorial Hospital has initiated Workplace Tobacco Cessation and Oral Cancer Screening Programme in Chemical Industry at Khed, Ratnagiri. Appropriate interventions for tobacco cessation will be carried at monthly intervals for twelve months duration. The tobacco cessation rates based on history will be validated with the urinary cotinine levels.

NCT ID: NCT00655421 Active, not recruiting - Oral Cancer Clinical Trials

Oral Cancer Screening in Mumbai, India by Primary Health Care Workers

Start date: April 2008
Phase: Phase 3
Study type: Interventional

A feasibility study to compare the test characteristics of three different oral cancer screening techniques performed by trained primary health care workers:1)Unaided Visual Inspection, 2)VelScope Assisted Examination, and 3) Examination after application of Toluidine Blue dye.

NCT ID: NCT00568490 Recruiting - Lung Cancer Clinical Trials

Identification of Secreted Markers for Tumor Hypoxia in Patients With Head and Neck or Lung Cancers

Start date: September 1, 1998
Phase:
Study type: Observational

The purpose of this study is to identify and confirm new blood and tissue markers for prognosis and tumor hypoxia. Tumor hypoxia, or the condition of low oxygen in the tumor, has been shown to increase the risk of tumor spread and enhance tumor resistance to the standard treatment of radiation and chemotherapy in head and neck and lung cancers. We have recently identified several proteins or markers in the blood and in tumors (including osteopontin, lysyl oxidase, macrophage inhibiting factor and proteomic technology) in the laboratory that may be able to identify tumors with low oxygen levels or more aggressive behaving tumors.

NCT ID: NCT00402779 Completed - Oral Cancer Clinical Trials

Erlotinib Prevention of Oral Cancer (EPOC)

Start date: November 3, 2006
Phase: Phase 3
Study type: Interventional

The goal of this clinical research study is to learn if erlotinib hydrochloride (Tarcevaâ (OSI-774 ) can prevent cancer in the mouth of people with a high risk of developing cancer in the mouth. The safety of this drug will also be studied, as well as the drug's effect on different cells in the body.

NCT ID: NCT00330382 Completed - Clinical trials for Oropharyngeal Cancer

Bowman-Birk Inhibitor Concentrate in Preventing Cancer in Patients With Oral Leukoplakia

Start date: January 1999
Phase: Phase 2
Study type: Interventional

This randomized phase II trial is studying how well Bowman-Birk inhibitor concentrate works in preventing cancer in patients with oral leukoplakia. Chemoprevention is the use of certain substances to keep cancer from forming, growing, or coming back. The use of Bowman-Birk inhibitor concentrate, a substance made from soy, may keep cancer from forming in patients with oral leukoplakia

NCT ID: NCT00186433 Completed - Clinical trials for Head and Neck Cancers

A Longitudinal Study of Plasma EBV DNA in Nasopharyngeal Carcinoma From Both Endemic and Non-Endemic Patient Populations

Start date: November 2001
Phase: N/A
Study type: Observational

1. To determine the prognostic implication of plasma Epstein-Bar Virus (EBV) DNA concentrations, as measured by quantitative polymerase chain reaction (PCR) in patients with nasopharyngeal carcinoma (NPC). 2. To relate pretreatment plasma EBV DNA concentration to WHO classification of these tumors both in endemic and non-endemic areas. 3. To determine whether pretreatment plasma EBV DNA can serve as a prognostic factor for both endemic and non-endemic patient populations.