Oropharyngeal Cancers Clinical Trial
— OP01Official title:
A Clinical Outcomes Protocol of Photon/Proton Beam Radiation Therapy for Oropharyngeal Cancers
Verified date | February 2017 |
Source | University of Florida |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this study is to collect information from the questionnaire and medical records to see what effects proton radiation has on cancer and collect and analyze morbidity outcomes: incidence of xerostomia (dry mouth) and tumor control.
Status | Terminated |
Enrollment | 10 |
Est. completion date | July 2015 |
Est. primary completion date | July 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Biopsy-proven squamous cell carcinoma of oropharynx (tonsillar pillars, tonsillar fossa, soft palate, base of tongue). - Stage-grouping: - Stage I (T1N0) - Stage II (T2N0) - Favorable Stage III (T1N1/T2N1) and selected stage IV (T1-T2 early N2b)2 or less lymph node and 2 or less cm diameter lymph node - Unfavorable stage III and selected stage IV (any T, N2c/N3) - Surgery of the primary tumor/lymph nodes is limited to incisional/excisional biopsies. - Will receive treatment with proton radiation. Exclusion Criteria: - Evidence of distant metastasis. - Previous irradiation for head and neck cancer. |
Country | Name | City | State |
---|---|---|---|
United States | University of Florida Proton Therapy Institute | Jacksonville | Florida |
Lead Sponsor | Collaborator |
---|---|
University of Florida |
United States,
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* Note: There are 23 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Collect and analyze morbidity outcomes: incidence of xerostomia | From date of registration until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 60 months | ||
Secondary | Collect and analyze tumor control outcomes. | From date of registration until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 60 months |