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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: NCT01927744 Recruiting - Clinical trials for Head and Neck Cancer

Study of Chemotherapy With Cisplatin/Carboplatin, and Docetaxel With or Without Erlotinib in Patients With Head and Neck Squamous Cell Carcinomas Amenable for Surgical Resection

Start date: December 16, 2013
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if adding erlotinib to a standard chemotherapy combination (docetaxel and either cisplatin or carboplatin) can help to control SCCHN. The safety of this drug combination will also be studied. In this study, erlotinib will be compared to a placebo. A placebo is not a drug. It looks like the study drug but is not designed to treat any disease or illness. It is designed to be compared with a study drug to learn if the study drug has any real effect. This is an investigational study. Erlotinib is approved by the FDA for treatment of non-small cell lung cancer. Its use in this study is experimental. Docetaxel, cisplatin, and carboplatin are all FDA approved and commercially available for the treatment of SCCHN. Up to 100 patients will take part in this study. All will be enrolled at MD Anderson.

NCT ID: NCT01911598 Completed - Clinical trials for Head and Neck Cancer

A Study of MEHD7945A in Combination With Cisplatin and 5-Fluorouracil (5-FU) or Paclitaxel and Carboplatin in Participants With Recurrent/Metastatic Squamous Cell Carcinoma of the Head and Neck (R/M SCCHN)

Start date: September 19, 2013
Phase: Phase 1
Study type: Interventional

This open-label, multicenter study will evaluate the safety, tolerability, and pharmacokinetics of MEHD7945A in combination with chemotherapy (either cisplatin plus 5-FU or carboplatin plus paclitaxel) in participants with previously untreated R/M SCCHN. There are two stages for each arm in this study: a Dose-limiting Toxicity (DLT)-evaluation stage (Stage I) and a cohort-expansion stage (Stage II). In Stage I, DLTs will be assessed during a DLT Assessment Window of 21 days (i.e., Cycle 1 Day 1 through Cycle 1 Day 21) for both arms. In Stage II, participants will be enrolled to further characterize the safety, pharmacokinetics, and anti-tumor activity of MEHD7945A in combination with cisplatin + 5-FU or carboplatin + paclitaxel at the identified recommended Phase II dose.

NCT ID: NCT01895829 Terminated - Clinical trials for Head and Neck Cancer

Ferumoxytol - Iron Oxide Nanoparticle Magnetic Resonance Dynamic Contrast Enhanced MRI

Start date: September 12, 2013
Phase: Early Phase 1
Study type: Interventional

The goal of this clinical research study is to learn if ferumoxytol, when given at the time of a magnetic resonance imaging (MRI), can help researchers learn more about the spread of certain kinds of cancers. Ferumoxytol is designed to deliver iron to treat iron-deficiency anemia (low red blood cell counts) in patients with chronic kidney disease. In this study, it will be used as an MRI contrast. Contrasts are used by doctors in order to see MRI images more clearly.

NCT ID: NCT01879384 Completed - Clinical trials for Head and Neck Cancer

Monitoring of Bone Free Flaps With Microdialysis

MTM
Start date: February 2011
Phase: N/A
Study type: Interventional

Microdialysis is admitted to be reliable by numerous surgeons to monitor flaps. Nevertheless, a few authors reported follow up with microdialysis in bone flaps, and they all described the position of the catheter in the surrounding soft tissue muscle. This surrounding soft tissue is not always the reflect of bone vascularisation. The aim is to study the feasibility of a follow up of microanastomosed bone flaps with microdialysis. To reach this goal, investigators perform a clinical prospective research project untitled MTM project

NCT ID: NCT01874860 Completed - Colorectal Cancer Clinical Trials

Skin Rash Study Before Chemotherapy in Colorectal & Head and Neck Cancer Patients

Start date: August 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if using preventive treatments such as Doxycycline (an anti-biotic) capsules, sunscreen with SPF 30, Hydrocortisone 1% cream and a moisturizer will help to reduce the incidence and severity of the skin rash associated with Cetuximab (Erbitux®) when compared to receiving standard care for the treatment of skin rash.

NCT ID: NCT01871311 Terminated - Colorectal Cancer Clinical Trials

A Phase I Study of Nilontinib and Cetuximab in Patients With Solid Tumors

Start date: May 2014
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the recommended Phase II dose of nilotinib when used in combination with cetuximab in the treatment of patients with recurrent and/or metastatic Kras wildtype colorectal cancer or squamous cell carcinoma of the head and neck.

NCT ID: NCT01871155 Completed - Clinical trials for Head and Neck Cancer

Effect of Nutri-jelly on Quality of Life in Head and Neck Cancer Patients

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

The purpose of this study is to determine whether a novel edible nutritious gel for patients with chewing and swallowing difficulties, Nutri-jelly, is effective in improving the quality of life of head and neck cancer patients while undergoing conventional radiotherapy.

NCT ID: NCT01846286 Active, not recruiting - Clinical trials for Head and Neck Cancer

Neuropathic Pain in Head and Neck Cancer

Start date: October 15, 2012
Phase:
Study type: Observational

The goal of this research study is to learn more about chronic pain associated with cancer treatment.

NCT ID: NCT01844557 Active, not recruiting - Clinical trials for Head And Neck Cancer

Testing Accountability in Patient Adherence

Start date: May 2013
Phase:
Study type: Observational

The goal of this research study is to look for factors that influence whether or not head and neck cancer patients follow the swallowing exercises that they are asked to perform while receiving radiation treatment.

NCT ID: NCT01843673 Active, not recruiting - Clinical trials for Head and Neck Cancer

Image-Guided Adaptive Radiotherapy for in Detecting Tumors During Treatment in Patients With Head and Neck Cancer

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

This clinical trial studies image-guided adaptive radiotherapy in detecting tumors during treatment in patients with head and neck cancer. Image-guided adaptive radiotherapy uses high quality imaging technology to detect the tumor and normal organs during treatment. It is not yet known which imaging technique provides the best image for guidance during treatment with radiation therapy. Comparing results of imaging procedures done before, during, and after radiotherapy may help doctors plan the best treatment.