MedPath

Identifying Prostate Brachytherapy Seeds Using MRI

Not Applicable
Completed
Conditions
Prostate Cancer Patients Who Have Brachytherapy Seed Implant
Interventions
Other: MRI Scan
Registration Number
NCT01878058
Lead Sponsor
University Health Network, Toronto
Brief Summary

This study will look at the feasibility of using a type of Magnetic Resonance Imaging called Susceptibility Weighted Imaging (SWI) to detect your implanted radioactive seeds. Researchers hope that using SWI will eliminate the need to use CT imaging to detect your implanted radioactive seeds.

This study will also see if the MRI seed detection is as effective as current standard practice of seed detection (routine MRI and CT imaging). This technique would be beneficial for brachytherapy without the need to fuse the MRI and CT images, as is done currently.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
10
Inclusion Criteria
  1. At least 18 years old
  2. Histologic diagnosis of adenocarcinoma of the prostate
  3. No contraindications for Pelvic body MRI
  4. Patients undergoing LDR brachytherapy at PMH and scheduled for post implant analysis with CT-MR (standard at PMH)
  5. Ability to provide written informed consent to participate in the study
Exclusion Criteria
  1. Contraindication for Pelvic body MRI
  2. Patient not willing/consenting for this study

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
MRI ScanMRI ScanPatients will receive an extra MRI scan in addition to their routine scan.
Primary Outcome Measures
NameTimeMethod
Determine if using the MR scan -(SWI) used to detect the implanted radioactive seeds will reduce registration errors6 months
Determine if using the MR scan -(SWI) used to detect the implanted radioactive seeds will reduce planning time for the post-implant plan6 months
Determine if using the MR scan -(SWI) used to detect the implanted radioactive seeds will eliminate the CT scan of the patient.6 months
Secondary Outcome Measures
NameTimeMethod
Compare the differences in MR seed identification using the MR pulse sequence vs. CT images.6 months

Our goal is to perfectly match these two modalities with acceptance test of 97%. This technique would be beneficial for LDR (Low Dose Rate) Brachytherapy without need to fuse the CT and MR images and eliminate any image registration uncertainly.

Trial Locations

Locations (1)

University Health Network, The Princess Margaret

🇨🇦

Toronto, Ontario, Canada

© Copyright 2025. All Rights Reserved by MedPath