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Clinical Trials/NCT00797602
NCT00797602
Completed
Not Applicable

A Clinical Outcomes Protocol of Proton Beam Radiation Therapy for Chordomas and/or Chondrosarcomas of the Base of Skull and/or Spine

University of Florida1 site in 1 country189 target enrollmentJanuary 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chordomas
Sponsor
University of Florida
Enrollment
189
Locations
1
Primary Endpoint
Collect and analyze outcome data on tumor control.
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The purpose of this study is to collect information from medical records to see what effects proton beam radiation has on cancer and analyze possible side effects.

Detailed Description

Data collection will be obtained from the patient's medical records including initial evaluation, pathology report, dosimetry information, radiotherapy completion records and follow-up.

Registry
clinicaltrials.gov
Start Date
January 2007
End Date
December 2015
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Histologically proven chordoma or chondrosarcoma.
  • Sites: base of skull and/or spine.
  • Age 18 years or older.

Exclusion Criteria

  • Previous radiation to the head and neck or brain.
  • Evidence of metastatic disease.

Outcomes

Primary Outcomes

Collect and analyze outcome data on tumor control.

Time Frame: When each patient has been followed for a minimum of 12 month and then again after 24 months to a maximum of 10 years.

Secondary Outcomes

  • Collect and analyze data on normal tissue morbidity.(When each patient has been followed for a minimum of 12 months and then again after 24 months to a maximum of 10 years.)

Study Sites (1)

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