Clinical Trials Directory

Trials / Completed

CompletedNCT01899404

MRI FDG PET Imaging Cervix

A Pilot Prospective Study of the Utility of Dynamic Contrast-Enhanced Magnetic Resonance Imaging (DCE-MRI), Diffusion Weighted MRI (DWI)and Positron Emission Tomography (PET) Imaging With 18F-Fluorodeoxyglucose (18FDG) in Brachytherapy for Cervix Cancer

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
25 (actual)
Sponsor
University Health Network, Toronto · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The standard treatment for cervix cancer at Princess Margaret Hospital is external radiation with chemotherapy followed by internal radiation, called brachytherapy. Currently, brachytherapy treatment is planned on a type of Magnetic Resonance Imaging (MRI) called T2-weighted (T2W) MRI. The main purpose of this study is to determine whether the following imaging tests can visualize the tumor better for planning the brachytherapy treatment: 1. special types of MRI called diffusion weighted MRI (DWI) and dynamic-contrast enhanced MRI (DCE-MRI); and 2. an x-ray test called positron emission test (PET) performed with a sugar dye called FDG. MRI-guided brachytherapy is resource-intensive and not widely available.

Conditions

Interventions

TypeNameDescription
BIOLOGICAL18-FDG PET/CT, DWI, DCE-MRIAll patients on this study will receive a Diffuse Weighted MRI and Dynamic Contrast Enhancing MRI during the routine MRI session on the day of brachytherapy (additional 10 minutes), and a FDG PET/CT scanning session on the day of brachytherapy.

Timeline

Start date
2012-10-03
Primary completion
2016-12-01
Completion
2016-12-01
First posted
2013-07-15
Last updated
2022-11-08

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01899404. Inclusion in this directory is not an endorsement.