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Sponsored by: |
Alberta Cancer Board |
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Information provided by: | Alberta Cancer Board |
ClinicalTrials.gov Identifier: | NCT00314496 |
Retrospectively have access to MR images of patients to develop software that:
The project involves software development of data that is already available. No intervention is made at this point.
Condition |
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Healthy |
Study Type: | Observational |
Study Design: | Retrospective |
Official Title: | Development of MR Simulation for Treatment Planning |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Adult patient with conform histological diagnosis of glioblastoma multiforme signed the consent forms and were willing to go for curative radiation treatment with temozolomide
Inclusion Criteria:
Contact: Gino Fallone, PhD | 780-432-8750 | ginofall@cancerboard.ab.ca |
Canada, Alberta | |
Cross Cancer Institute | Recruiting |
Edmonton, Alberta, Canada, T6G 1Z2 | |
Contact: Clinical Research Unit 780-989-8152 clinical_trials_cci@cancerboard.ab.ca | |
Principal Investigator: Gino Fallone, PhD |
Principal Investigator: | Gino Fallone, PhD | Alberta Cancer Board |
Responsible Party: | Alberta Cancer Board ( Gino Fallone ) |
Study ID Numbers: | EX-0004 |
Study First Received: | April 11, 2006 |
Last Updated: | September 22, 2008 |
ClinicalTrials.gov Identifier: | NCT00314496 |
Health Authority: | Canada: Health Canada |
Healthy |