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CT/MRI Co-registration Prostate Cancer

University Health Network, Toronto logo

University Health Network, Toronto

Status

Completed

Conditions

Prostatic Neoplasm

Treatments

Device: Computed Tomography Scan and Magnetic Resonance Imaging

Study type

Observational

Funder types

Other

Identifiers

NCT00252460
UHN REB 03-0601-CE

Details and patient eligibility

About

The target volume in prostate cancer radiotherapy typically consists of the entire prostate gland which is localized by contours drawn on axial computed tomography (CT) radiation planning images. Compared with CT, magnetic resonance (MR) can provide better definition of the prostate gland with respect to the surrounding tissues and the use of multi-plannar reconstruction avoids the problem of partial volume averaging inherent in CT. CT has been shown to significantly overestimate the volume of the gland using the MR-defined prostate volume as the gold standard. Co-registration of MR and CT datasets, matched on fixed bony landmarks, has enabled radiation planning using a MR-defined clinical target volumes, combined with CT-based electron density information necessary for radiation treatment planning.

Rationale and Hypothesis:

Co-registration may allow better delineation of tumour volumes in prostate cancer. This investigation is a fesibility study designed to evaluate and optimize imaging parameters and co-registration techniques for CT planning and MRI Simulator.

Enrollment

31 patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Histological confirmation of Prostate Adenocarcinoma
  • Undergoing RT with fiducial markers, IMRT or Escalated Dose Conformal RT

Exclusion criteria

  • Contraindication for MRI

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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