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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00126854
Other study ID # NA-15-0003 / 22011
Secondary ID
Status Completed
Phase N/A
First received August 3, 2005
Last updated February 24, 2016
Start date October 2005
Est. completion date April 2011

Study information

Verified date March 2012
Source AHS Cancer Control Alberta
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Interventional

Clinical Trial Summary

The purpose of this study is to establish the correct scanning parameters for obtaining good quality 3 Tesla (3T) magnetic resonance spectroscopy images (MRSI) of the prostate gland before and after brachytherapy implantation for prostate cancer. Three Tesla MRSI may be a valuable additional diagnostic and follow-up investigation for prostate cancer patients.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date April 2011
Est. primary completion date April 2011
Accepts healthy volunteers No
Gender Male
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Suitable candidate for prostate brachytherapy to treat prostate cancer

- Patient signs a study consent form

Exclusion Criteria:

- Have received other radiotherapy for prostate cancer or hormone treatments

- Has contraindication to MRSI scanning

- Does not sign study consent form

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Procedure:
Magnetic Resonance Spectroscopy Imaging


Locations

Country Name City State
Canada Cross Cancer Institute Edmonton Alberta

Sponsors (2)

Lead Sponsor Collaborator
AHS Cancer Control Alberta Cross Cancer Institute

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary pilot study meant to establish scanning parameters on 3T MRSI
Secondary safety/toxicity
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