Temporal Pattern of Circulating DNA for Patients Receiving Irradiation

Terminated

• Conditions: Radiation

• Registration Number: NCT01099020
• Lead Sponsor: University of Rochester

Brief Summary

The purpose of the research study is to test a measurement tool that will determine the radiation dose people receive when they have been accidentally exposed to radiation. This test will be done using a small amount of blood and known dose of radiation.

Detailed Description

Not available

Study Timeline

• Study Start: 2010-04
• Study First Submitted: 2010-04-02
• Study First Submitted QC: 2010-04-05
• Study First Posted: 2010-04-06
• Primary Completion: 2011-12
• Study Completion: 2011-12
• Status Verified: 2015-05
• Last Update Submitted: 2015-05-29
• Last Update Posted: 2015-06-02

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 13

Inclusion Criteria

• Patient must be scheduled to undergo Total Body Irradiation (TBI) as part of a conditioning regime for a Bone Marrow Transplant. OR, Be scheduled to undergo Radiation Therapy treatment for a malignancy or other disease and have a radiation treatment field that contains at least 2 liters of tissue receiving at least 2 Gy radiation dose over the first 5 days of treatment.
• Patient must be willing to have blood draws as defined below.
• Patient must provide study-specific informed consent prior to study entry.
• Hemoglobin≥8.
• Age ≥ 18, but not older than age 60.

Exclusion Criteria

• Patients not meeting the above inclusion criteria.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Trial Locations

Locations (1)

University of Rochester; 🇺🇸 Rochester, New York, United States