Clinical Trials Logo

Clinical Trial Summary

To verify and validate a biodosimetry test for determining absorbed ionizing radiation dose by analyzing gene expression signatures of blood samples collected from patients treated with Total Body Irradiation (TBI).


Clinical Trial Description

In order validate the performance of DxTerity's Radiation Biodosimetry Test (RBT) system, several clinical centers will provide controlled, de-identified blood samples and associated clinical information to DxTerity Diagnostics (DxTerity). Variations in dose and frequency of delivery in TBI protocols are expected between the clinical centers and this has been accounted for in the study design. Samples from up to 200 participants will be collected via this protocol. Blood samples for this study will be collected from radiation therapy patients receiving TBI as part of a therapeutic regimen from the site. Blood samples (up to 4 mL per time point) may be obtained at the time of routine blood collection; participation in this biomarker study will not affect any aspect of patient treatment. Study samples will be obtained prior to, during, and post-radiation treatment regimen. Associated clinical information will be collected from the subject's medical record, as well. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03123133
Study type Observational
Source DxTerity Diagnostics
Contact
Status Completed
Phase
Start date April 6, 2017
Completion date July 14, 2020

See also
  Status Clinical Trial Phase
Completed NCT02670252 - BuCY vs TBICY Conditioning Regimen for Standard-risk ALL Undergoing Allo-HSCT Phase 3