Protocol Details
Evaluation of Late Effects and Natural History of Disease in Patients Treated with Radiotherapy
This study is currently recruiting participants.
Summary
Number | 00-C-0074 |
Sponsoring Institute | National Cancer Institute (NCI) |
Recruitment Detail | Type: Participants currently recruited/enrolled
Gender: Male & Female
Min Age: 18 Years
Max Age: N/A |
Referral Letter Required | No |
Population Exclusion(s) | Children |
Keywords | Late Effects;
Radiation Therapy;
Cancer;
Natural History |
Recruitment Keyword(s) | None |
Condition(s) | Cancer |
Investigational Drug(s) | None |
Investigational Device(s) | None |
Intervention(s) | None |
Supporting Site | National Cancer Institute |
BACKGROUND
-This protocol acknowledges that it is in the interest of the NIH and ROB, as well as our participants, to continue to follow those who have been treated with radiotherapy at ROB and are not otherwise eligible for current active research protocols.
-It also provides a mechanism for the correlation and interpretation of disparate data for research into the long term side effects and outcomes for a variety of disease entities and treatments, such as combined modality treatment, MoAb, PDT, radiation modifiers,
intraoperative radiotherapy, etc.
OBJECTIVE
-The primary objective of this protocol is to assess the late effects of treatment and the natural history of disease through collection of data from any standard procedures performed as part of follow up care on participants previously treated with radiotherapy.
ELIGIBILITY
-Participants who received radiation therapy.
DESIGN
-This is a natural history protocol in which long-term follow up data will be collected from participants who received radiation therapy.
-It will be made clear to participants in the consent form, that data collected during their follow-up may be used anonymously for publications concerning the natural history of disease processes and long-term effects of treatment.
Eligibility
INCLUSION CRITERIA:
ROB investigator deems that it is in the best interests of the participant and the NCI/ROB for the participant to be seen in follow-up in the ROB clinic.
Participant is able to provide informed consent.
Participant must have a primary physician in the community to whom records and appropriate follow-up management can be given. Social services will be enlisted for any participants who lack health insurance, etc.
Participants who have received radiotherapy.
Age greater than or equal to 18 years of age
EXCLUSION CRITERIA:
Participants who are on an interventional research protocol at NIH at the time of enrollment.
Citations:
Not Provided
Contacts:
Clinical Trials Number:
NCT00026650