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Trial record 24 of 3446 for:    Facility

Receiving Radiation Therapy in the MRgRT Research Facility (MRgRT)

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ClinicalTrials.gov Identifier: NCT02701712
Recruitment Status : Recruiting
First Posted : March 8, 2016
Last Update Posted : April 26, 2019
Sponsor:
Information provided by (Responsible Party):
University Health Network, Toronto

Brief Summary:
The aim of this study is to evaluate the technical performance of magnetic-resonance guided radiotherapy (MRgRT) facility at the Princess Margaret Cancer Centre and the impact on the workflow of the clinical team in this facility.

Condition or disease Intervention/treatment Phase
Solid Tumors and Metastatic Lesions Radiation: Magnetic resonance - guided radiation therapy (MRgRT) Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 150 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Receiving Radiation Therapy in the MRgRT Research Facility
Study Start Date : February 2016
Estimated Primary Completion Date : February 2020
Estimated Study Completion Date : February 2021

Arm Intervention/treatment
Experimental: Magnetic resonance - guided radiation therapy (MRgRT)
Magnetic resonance (MR) - guided radiation therapy
Radiation: Magnetic resonance - guided radiation therapy (MRgRT)
Use of magnetic resonance (MR) visualization for interventional radiotherapy in cancer patients




Primary Outcome Measures :
  1. Proportion of planned patients receiving treatment in the MRgRT facility [ Time Frame: 2 years ]

Secondary Outcome Measures :
  1. Measure tumor size before, during and after radiotherapy [ Time Frame: 2 years ]
    Collect and analyze imaging data before, during and after radiotherapy, and the related treatment data



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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Ability to provide informed consent
  • Planned to receive clinical intervention (imaging or treatment) in the MRgRT facility
  • At least 18 years of age

Exclusion Criteria:

-


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02701712


Contacts
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Contact: Michael Milosevic, MD 416-946-4501 ext 2932 mike.milosevic@rmp.uhn.on.ca

Locations
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Canada, Ontario
University Health Network Recruiting
Toronto, Ontario, Canada, M5G 2M9
Contact: Mike Milosevic, MD    416-946-4501 ext 2932    mike.milosevic@rmp.uhn.on.ca   
Principal Investigator: Mike Milosevic, MD         
Sponsors and Collaborators
University Health Network, Toronto
Investigators
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Principal Investigator: Michael Milosevic, MD University Health Network, Toronto

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Responsible Party: University Health Network, Toronto
ClinicalTrials.gov Identifier: NCT02701712     History of Changes
Other Study ID Numbers: 14-8210-CE
First Posted: March 8, 2016    Key Record Dates
Last Update Posted: April 26, 2019
Last Verified: April 2019
Keywords provided by University Health Network, Toronto:
magnetic resonance
external beam radiotherapy
brachytherapy
radiotherapy