Data Collection to Assess Acute and Late Normal Tissue Sequelae in Proton Therapy for Adults

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
United States
Texas
M D Anderson Cancer Center
RECRUITING
Houston
Contact Information
Primary
Steven J. Frank
sjfrank@mdanderson.org
713-563-2300
Time Frame
Start Date: 2005-05-27
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 5000
Treatments
Observational (questionnaire)
Patients undergoing standard of care proton therapy are assessed for toxicities weekly during proton treatment, then from 1 to 3 times up to 90 days from the start of treatment and annually thereafter. Patients also complete questionnaires over 15-20 minutes at baseline, weekly during treatment, and every 2 weeks during follow up for up to 3 months.
Sponsors
Leads: M.D. Anderson Cancer Center

This content was sourced from clinicaltrials.gov

Similar Clinical Trials