Clinical Trials Directory

Trials / Completed

CompletedNCT00252460

CT/MRI Co-registration Prostate Cancer

Evaluation of Planning Computed Tomography Scan and Magnetic Resonance Imaging Simulator Scan Co-Registration for Delineation of Gross Tumour Volume in Radiotherapy Treatment of Localized Prostate Cancer

Status
Completed
Phase
Study type
Observational
Enrollment
31 (actual)
Sponsor
University Health Network, Toronto · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DEVICEComputed Tomography Scan and Magnetic Resonance Imaging

Timeline

Start date
2003-11-01
Primary completion
2010-11-01
Completion
2010-11-01
First posted
2005-11-11
Last updated
2016-03-25

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00252460. Inclusion in this directory is not an endorsement.