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Dynamic Contrast Enhanced MRI (DCE-MRI) Diffusion Weighted MRI (DW-MRI) and Magnetic Resonance Spectroscopy (MRS) of Head and Neck Tumors

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City:   New York
State:   New York
Zip Code:   10065
Conditions:   Head and Neck Cancer
Purpose:   Magnetic resonance imaging (MRI) is a diagnostic study that makes pictures of organs of the body using magnetic field and radio frequency pulses that can not be felt. Dynamic contrast enhanced-magnetic resonance imaging (DCE-MRI) uses faster imaging and contrast material (a substance used to make specific organs, blood vessels, or tumors easier to see) that is given by vein. Diffusion weighted magnetic resonance imaging (DW-MRI) allows to measure the motion of water around the cells in the tumor. Proton magnetic resonance spectroscopy (MRS) obtains chemical information from the tumor. During MRS, signals are detected from the chemicals (spectroscopy) naturally present in your tumor using radio waves. DCE-MRI, DW-MRI and MRS give extra information which is not available with the regular MRI. The regular MRI only shows pictures of the tumor while the DCE-MRI also gives information about the blood vessels of the tumor. DW-MRI provides information related to the state of the tumor tissue with regards to the quality or condition of cells present in it and MRS gives information about the chemical makeup of the tumor. The purpose of this study is to see whether DCE-MRI, DW-MRI and MRS done before treatment can predict which patients will do well with either surgery or chemo-radiation therapy. This study will also see if DCE-MRI, DW-MRI and MRS done early in treatment can tell if the therapy is working.
Study Summary:  
Criteria:   Inclusion Criteria: - Patients with histologically proven diagnosis of head and neck cancer or patients with tumors strongly suspicious for head and neck cancer due to clinical features or FNA (fine needle aspiration) cytology assessment. - Will undergo surgery or chemo-radiation treatment - Presence of evaluable primary tumor - Patients must be 18 years or older and have the ability to give informed consent Exclusion Criteria: - Claustrophobia - Absence of evaluable primary tumor - Known reaction to Gd-DTPA - Pre-operative radiation to primary tumor site - Contraindication to MRI 1. Pacemaker 2. Aneurysmal clips 3. Metal implants in field of view 4. Pregnant or nursing women 5. Age and mental status wherein he/she is unable to cooperate for MRI study
NCT ID:   NCT00581906
Primary Contact:   Principal Investigator
Amita Dave, PhD
Memorial Sloan-Kettering Cancer Center

Amita Dave, PhD
Phone: 212-639-3184
Backup Contact:   Hilda Stambuk,, MD
Phone: 212-639-2728
Location Contact:   New York, New York 10065
United States

Amita Dave, PhD
Phone: 212-639-3184

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   May 23, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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