Clinical

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Study of the use of MRI for radiation therapy treatment planning for patients with complex pelvic cancers


ABSTRACT: Interventions: The study involves an additional MRI scan being required for the study. This will require attendance at one MRI scan session of a half hour duration from the participant. This modification does not affect the gold standard of imaging the patients would otherwise receive for their treatment. This MRI scan will be undertaken at the Diagnostic Imaging Department, Calvary Mater Newcastle, scheduled on the same day as the participants planning CT scan. There will be no change to the participant’s treatment in this study – they will receive the gold standard of care and treatment as per departmental protocols. The MRI scan will be used for comparative purposes only. The MRI will be used to create a synthetic CT scan which will be used prospectively to compare to the participants previously acquired CT scan Primary outcome(s): This is a composite primary outcome to demonstrate the mean dosimetric agreement and 95% confidence interval between conventional CT and synthetic CT for radiotherapy treatment planning of cancers of the rectum, anal canal, endometrium and cervix[after completion of radiotherapy treatment planning]

DISEASE(S): Cancer-womb (uterine Or Endometrial Cancer),Endometrial Cancer,Cancer-bowel-anal,Cervical Cancer,Anal Canal Cancer,Cancer-cervical (cervix),Cancer-bowel-back Passage (rectum) Or Large Bowel (colon),Rectal Cancer

PROVIDER: 2466170 | ecrin-mdr-crc |

REPOSITORIES: ECRIN MDR

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