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Head and Neck Cancer clinical trials

View clinical trials related to Head and Neck Cancer.

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NCT ID: NCT01663246 Completed - Clinical trials for Head and Neck Cancer

Cross-Sectional Study of Oral Health in Patients After Parotid-Sparing Radiation Therapy for Head and Neck Cancer

Start date: April 2006
Phase: N/A
Study type: Interventional

The investigators are conducting research about oral health and saliva to find out more about the impact of radiation therapy on the oral health of patients. In order to better understand the role of saliva in maintaining oral health in these patients, the investigators will be collecting, storing, and analyzing the quality of saliva, including the protein content, collected from patients following radiation therapy as well as saliva collected from normal healthy adults.

NCT ID: NCT01661062 Active, not recruiting - Clinical trials for Head and Neck Cancer

A Study Using Cone Beam CT for Head and Neck Cancer

Start date: January 2009
Phase: N/A
Study type: Interventional

Cone beam CT (computed tomography) is a developing technology which allows CT images to be obtained while a patient is on the radiation treatment table.(A CT scan uses x-rays to produce detailed pictures of structures in the body.) In this study, cone beam CT scans will be obtained before individual radiation treatment sessions for head and neck cancer. The information gathered from these scans will be used by the researchers to look at patient movement as well as changes in the amount of normal and tumor tissue throughout the course of radiation therapy. The researchers will use this information to create hypothetical radiation treatment plans, which will be used as the basis for future research. The cone beam CT scan data will not be used to alter the actual radiation treatment of any of the patients enrolled on the study. In addition, tests of salivary output and swallowing and questionnaires about quality of life will be made to assess how the doses of radiation affect them.

NCT ID: NCT01653327 Completed - Clinical trials for Head and Neck Cancer

Analgesic Effects of Topical Ketamine Mouthwash in Patients Receiving Chemoradiation or Radiotherapy for Head & Neck Cancer

Start date: June 2010
Phase: Phase 2
Study type: Interventional

- The primary objective is to determine the reduction in pain score by ketamine mouthwash compared to placebo in head and neck cancer patients with refractory mucositis. - The secondary objectives are to describe the duration of analgesia and adverse effects associated with ketamine and placebo.

NCT ID: NCT01652456 Withdrawn - Lung Cancer Clinical Trials

Alcohol and Tobacco Consumption in Patients With Head and Neck Cancer : Interest of an Addiction Support

Start date: October 2012
Phase: N/A
Study type: Interventional

This is a multicenter, interventional, randomized study for preventive and therapeutic strategies for patients with head and neck or Lung cancer; contribution of an addiction support

NCT ID: NCT01649583 Completed - Clinical trials for Head and Neck Cancer

Feasibility Study of Dynasplint to Prevent Trismus in Head and Neck Cancer

Start date: August 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to see if use of a device called the Jaw Dynasplint® System can be used during and immediately after cancer treatment. The Dynasplint® is a stretching device that is used to treat joint stiffness and limited range of motion in the jaw. The device is currently approved for treatment of trismus once it has developed. This study will investigate the use of the device during and immediately after cancer treatment to prevent trismus.

NCT ID: NCT01647425 Completed - Lung Cancer Clinical Trials

Alcohol and Tobacco Consumption in Patients With Head and Neck or Lung Cancer

ALTAK
Start date: April 2012
Phase: N/A
Study type: Observational

This is an multicenter study for preventive and therapeutic strategies for patients with head and neck cancer

NCT ID: NCT01645748 Completed - Clinical trials for Head and Neck Cancer

Docetaxel, Cisplatin, and S-1 (TPS) Induction Chemotherapy in Locally Advanced Head and Neck Cancer

TPSHNSCC
Start date: October 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study was to evaluate the tolerability and efficacy of a combination of weekly docetaxel, cisplatin, and S-1 (weekly TPS) as induction chemotherapy in patients with locally advanced head and neck squamous cell carcinoma (HNSCC).

NCT ID: NCT01619618 Completed - Clinical trials for Head and Neck Cancer

Studying Biomarkers in Samples From Patients With Recurrent or Metastatic Head and Neck Cancer Treated on E1302 Trial

Start date: June 1, 2012
Phase: N/A
Study type: Observational

RATIONALE: Studying samples of blood and tissue from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors predict how patients will respond to treatment. PURPOSE: This laboratory study is looking at biomarkers in samples from patients with recurrent or metastatic head and neck cancer treated on ECOG-E1302 trial.

NCT ID: NCT01612351 Active, not recruiting - Clinical trials for Head and Neck Cancer

Multimodality Risk Adapted Tx Including Induction Chemo for SCCHN Amenable to Transoral Surgery

Start date: June 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to see if a three method risk adapted design using induction chemotherapy, transoral surgery and radiation chemotherapy will lessen toxic effects and make treatment of squamous cell carcinoma of the head and neck (SCCHN) better.

NCT ID: NCT01609114 Active, not recruiting - Clinical trials for Head and Neck Cancer

Irradiation Modulates the Pharmacokinetics of Anticancer Drugs for Head and Neck Cancer

Start date: April 2012
Phase: N/A
Study type: Observational

The concurrent use of chemotherapy during radiation therapy (CCRT) is now the important treatment stratagem for locally advanced head and neck cancer or nasopharyngeal cancer (NPC). For these cases, 5-Fluorouracil (5-FU) and cisplatin (CDDP) are the most commonly used agents of CCRT. It plays an important role to improve the treatment outcome and increases the opportunities for organ preservation. In the past, Radiotherapy (RT) was solely used as a local treatment and its effect was estimated by local effect model. However, growing evidence shows that irradiation has direct DNA damage-dependent effects as well as sending signals to neighboring cells. Recently, the investigators reported that abdominal irradiation could significantly modulate the systemic pharmacokinetics of 5-FU at 0.5 Gy, off-target area in clinical practice, and at 2 Gy, the daily treatment dose for target treatment in an experimental rat model. Additionally, the results from a clinical investigation showed that colorectal cancer patients with lower AUC of 5-FU during adjuvant chemotherapy had lower disease-free survival. Taken together, these lines of evidence support the importance and necessity to search for the mediators responsible for the unexpected effect of local RT on systemic pharmacokinetics of chemotherapeutic agents, such as 5-FU. In the present study, the investigators examined whether the phenomena and mechanism of RT-PK(pharmacokinetics) is a fact for different anticancer drugs and for different part in human.