Expired Study
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St. Louis, Missouri 63110


Purpose:

Patients with head and neck cancer and are schedule to receive standard radiation therapy known as IMRT to treat cancer


Study summary:

In this study, we will plan additional measurements of the position of the patient's organs weekly during radiation treatment. We will analyze these measurements in order to evaluate whether we need to adjust our treatment procedures for the remainder of the treatments. We might adjust the dose of radiation received to specific organs in order to try to minimize the amount of radiation the healthy tissue receives.


Criteria:

Inclusion Criteria: - Age >= 18 - Karnofsky Performance Status of >= 60 - New diagnosis of head-and-neck cancer, all subsites included (i.e. nasopharynx, oropharynx, oral cavity, hypopharynx, larynx.) - All stages with measurable gross disease (>= 1.0 cm) by CT imaging - Pathologic confirmation of squamous cell carcinoma by biopsy or cytology - Signed study-specific consent form - Sequential or concurrent chemotherapy is allowed but not mandated. (no chemotherapy is allowed if patient is judged not to be a candidate for chemotherapy by the medical oncologist) Exclusion Criteria - Age < 18 - Karnofsky Performance Status < 60 - Radiographic or pathologic evidence of distant metastatic disease (i.e. other than cervical lymph nodes) - Prior radiation therapy to the head-and-neck region


NCT ID:

NCT00608751


Primary Contact:

Principal Investigator
Wade Thorstad, MD
Washington University School of Medicine


Backup Contact:

N/A


Location Contact:

St. Louis, Missouri 63110
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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