Data Collection for the Assessment of Acute and Late Normal Tissue in Patients Treated With Proton Therapy
Recruiting · NCT00991094 · Observational (researchers observe without assigning treatment) · Lead sponsor: M.D. Anderson Cancer Center
View the official record on ClinicalTrials.gov →Interventions studied
Quality-of-Life AssessmentQuestionnaire Administration
What this trial is about
This study collects information on the side effects of proton therapy and detailed information on the proton therapy treatment plan itself. This may help researchers develop methods to predict the risk of side effects for future patients and learn the long-term benefit of proton therapy.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- All patients scheduled for radiation treatment with protons at UTMDACC are eligible for this protocol
- Patients must sign a study-specific consent form prior to study entry
Exclusion criteria
- Patients who are unable or unwilling to attend the required periodic follow-ups either at M.D. Anderson or at a different site
Where it is running
2 locations listed across 1 US state.
- M D Anderson Cancer Center - Houston, Texas, United States
- M D Anderson Cancer Center - Houston, Texas, United States