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Head and Neck Neoplasms clinical trials

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NCT ID: NCT01354548 Active, not recruiting - Trismus Clinical Trials

Prevention of Trismus During Radiotherapy and Quality of Life in Head and Neck Cancer Patients

Start date: February 2010
Phase: N/A
Study type: Interventional

Trismus (limited jaw mobility), can occur in patients undergoing radiotherapy to specific areas of the head or neck. Trismus leads to difficulty in eating, swallowing, speech and general mouth hygiene, which all have negative effects on quality of life. Research in the area of trismus is limited; it is not known exactly when trismus develops, one study suggests that some patients have experienced a diminished opening at as low doses as 15 Gy. Literature suggests benefits of a training programme, but there is a lack of evidence to support the use of a training programme during radiotherapy. The purpose of this study is to investigate the effectiveness of a training programme during and after radiotherapy, and report the incidence of trismus in patients who receive radiotherapy to the jaw muscles. The study also investigates quality of life during radiotherapy and up to one year after completed treatment. Patients who meet the criteria and give their consensus to the study are divided into two groups: Group 1: Training with TheraBite Jaw Motion Rehabilitation System, which is a portable system utilizing repetitive passive motion and stretching to restore mobility and flexibility of the jaw musculature. Individuals train five times a day. Group 2: Conventional treatment (jaw measurements once a week). If the individuals jaw mobility decreases 15% from the original start measurement, the patient is automatically offered a trainings program (as in group 1). During radiation therapy a hospital specialist dentist measures the jaw mobility once a week, thereafter at 3,6,12 months after completed Radiation Therapy. On 5 different occasions the patients are requested to complete a Quality of life questionnaire. Patient's record their training frequency in a log book.

NCT ID: NCT01349309 Completed - Dysphagia Clinical Trials

The Effect of Prophylactic Swallowing Exercises on Head and Neck Cancer Patients

Start date: June 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to find out if doing prophylactic or preventative swallowing exercises from the start of cancer treatment can improve the ability to swallow when the treatment is completed and beyond.

NCT ID: NCT01347281 Completed - Clinical trials for Cancer of the Head and Neck

PET With [18F]HX4 in Head and Neck Cancer

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

The aim of this study is to (i) Determine if tumor hypoxia can be accurately visualised with [18F] HX4 PET imaging in head and neck tumors (ii) correlate the [18F] HX4 PET images with blood and tissue markers and (iii) investigate the quality and optimal timing of [18F] HX4 PET imaging (iv) compare [18F] HX4 PET uptake with [18F] FDG PET uptake before and after treatment.

NCT ID: NCT01345682 Completed - Clinical trials for Head and Neck Neoplasms

LUX-Head&Neck 1: A Phase III Trial of Afatinib (BIBW2992) Versus Methotrexate for the Treatment of Recurrent and/or Metastatic (R/M) Head and Neck Squamous Cell Cancer After Platinum Based Chemotherapy

Start date: January 5, 2012
Phase: Phase 3
Study type: Interventional

This randomised, open-label, phase III study will be performed in patients with R/M head and neck squamous cell carcinoma (HNSCC) who have progressed after platinum-based therapy. The objectives of the trial are to compare the efficacy and safety of afatinib versus methotrexate

NCT ID: NCT01345669 Terminated - Clinical trials for Head and Neck Neoplasms

LUX-Head&Neck 2: A Phase III Trial of Afatinib (BIBW 2992) Versus Placebo for the Treatment of Head and Neck Squamous Cell Cancer After Treatment With Chemo-radiotherapy

Start date: October 17, 2011
Phase: Phase 3
Study type: Interventional

This randomised, double-blind phase III trial will be performed in patients with head and neck squamous cell carcinoma (HNSCC). The objectives of the trial are to compare the efficacy and safety of afatinib (BIBW 2992) with placebo as adjuvant therapy to patients who have received definitive chemo-radiotherapy.

NCT ID: NCT01345084 Withdrawn - Clinical trials for Head and Neck Cancer

Study Comparing Radiation Therapy and Chemotherapy With or Without Nimotuzumab

NICAP
Start date: November 2013
Phase: Phase 3
Study type: Interventional

Primary: to compare the overall survival defined as the time elapsed between the randomization date and death due to any cause, in both treatment groups. Secondary: to compare the progression-free survival, incidence of locoregional failure, site of the first recurrence/progression, objective response rate assessment, quality of life assessment and incidence of adverse events.

NCT ID: NCT01344356 Completed - Clinical trials for Nasopharyngeal Carcinoma

Stereotactic Body Radiotherapy for Head and Neck Tumors

Start date: July 2008
Phase: Phase 4
Study type: Interventional

This study will evaluate the local control rates as well as acute and late toxicity rates of stereotactic body radiotherapy (SBRT) for the treatment of benign and malignant head and neck tumors.

NCT ID: NCT01341535 Completed - Clinical trials for Primary Non-operated Squamous Cell Carcinoma of Larynx

Comparison of Adaptive Dose Painting by Numbers With Standard Radiotherapy for Head and Neck Cancer.

C-ART-2
Start date: September 2011
Phase: Phase 2
Study type: Interventional

The investigators hypothesize that treatment adaptation to biological and anatomical changes, occurring during treatment, can increase the chance of cure at minimized or equal radiation-induced toxicity in head and neck cancer patients. This trial compares standard intensity-modulated radiotherapy (IMRT), using only pre-treatment planning 18F-2-fluoro-2-deoxy-D-glucose positron emission tomography to adaptive 18F-2-fluoro-2-deoxy-D-glucose positron emission tomography voxel intensity based IMRT or volumetric-modulated arc therapy (VMAT) using repetitive per-treatment planning 18F-2-fluoro-2-deoxy-D-glucose positron emission tomography for head and neck cancer.

NCT ID: NCT01333852 Terminated - Clinical trials for Head and Neck Neoplasms

Metformin Plus Paclitaxel for Metastatic or Recurrent Head and Neck Cancer

METTAX
Start date: February 2011
Phase: Phase 2
Study type: Interventional

Metformin plus paclitaxel for recurrent or metastatic head and neck cancer: a randomized phase II trial

NCT ID: NCT01333696 Recruiting - Clinical trials for Squamous Cell Carcinoma of Head and Neck

Pemetrexed as Salvage Treatment in Squamous Cell Carcinoma of Head and Neck

Start date: April 2011
Phase: Phase 2
Study type: Interventional

The aim of the study is to evaluate the efficacy and safety of pemetrexed monotherapy as salvage treatment in patients with relapsed or metastatic squamous cell carcinoma of head and neck.