Genomic Assessment of Patients With Severe Radiation Reactions

NCT03287349 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3

Last updated 2024-11-15

No results posted yet for this study

Summary

Determine an underlying etiology behind unexpectedly severe reactions to radiation by blood draw.

Conditions

  • Radiation; Reaction

Interventions

OTHER

Blood draw

Two 12.5 mL blood draws

OTHER

Photograph

Photograph of severe reaction, will be anonymized

DIAGNOSTIC_TEST

Autoimmune testing

Autoimmune testing in patients without prior testing

Sponsors & Collaborators

Principal Investigators

  • Kimberly Corbin, M.D. · Mayo Clinic

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-05-10
Primary Completion
2023-01-04
Completion
2023-01-04

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03287349 on ClinicalTrials.gov