Measuring Alterations of DNA in Human Blood
1 other identifier
observational
24
1 country
1
Brief Summary
The purpose of this research is to evaluate an automated, laser-based technique for measuring DNA damge resulting from radiation. We want to use controlled exposure on cancer patients to help develop a measurement to test people who may have been accidentally exposed to radiation.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 12, 2005
CompletedFirst Posted
Study publicly available on registry
September 15, 2005
CompletedSeptember 11, 2006
September 1, 2006
September 12, 2005
September 6, 2006
Conditions
Eligibility Criteria
You may qualify if:
- Male or female, age 21 to 70 years old.
- Patient undergoing with anti-neoplastic agent(s) known to have genotoxic activity (e.g., cyclophosphamide, 5-FU, cisplatin, Ara-C.
- X-irradiation may be considered, so long as a substantial fraction of red marrow is exposed (e.g., femur or chest/trunk region);
- treatment could be ongoing therapy or initial therapy.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Rochesterlead
- Litron Laboratoriescollaborator
Study Sites (1)
University of Rochester
Rochester, New York, United States
MeSH Terms
Conditions
Study Officials
- PRINCIPAL INVESTIGATOR
Yuhchyau Chen, MD, Ph.D
Universtiy of Rochester, Dept of Radiation Oncology
Study Design
- Study Type
- observational
- Observational Model
- DEFINED POPULATION
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
September 12, 2005
First Posted
September 15, 2005
Last Updated
September 11, 2006
Record last verified: 2006-09