CompletedNot Applicable

Radiotherapy Assessments During Intervention ANd Treatment (RADIANT)

United States16 participantsStarted 2017-04-06

Plain-language summary

Collect blood samples and associated clinical data prior to, during, and post radiation treatment.

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

✓. Male and female patients age 18 or older
✓. Have a permanent address in the United States for the duration of the study
✓. Diagnosed with a primary gastrointestinal (GI), genitourinary (GU), or gynecological (GYN) cancer
✓. Planned radiation therapy to the abdominal/pelvic area as part of clinical care
✓. Able to provide informed consent

Obtain pre- and post-irradiation participant-collect blood samples

Timeframe: 1.5 years

NCT IDNCT03133286

SponsorDxTerity Diagnostics

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2020-02-24