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Feasibility of Using Real-time Cine-MRI for Treating Moving & Deforming Tumors
Investigating the Feasibility of Using Real-time Cine-MRI for Treating Moving and Deforming Tumors
2 other identifiers
observational
5
1 country
1
Brief Summary
This study aims to investigate and optimize imaging sequences and parameters of rapid real-time MRI in order to obtain adequate guidance for accurately and precisely delivering radiation to moving abdominal and thoracic tumors.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Feb 2009
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2009
CompletedFirst Submitted
Initial submission to the registry
December 16, 2009
CompletedFirst Posted
Study publicly available on registry
February 19, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2010
CompletedDecember 7, 2012
December 1, 2012
1.6 years
December 16, 2009
December 5, 2012
Conditions
Outcome Measures
Primary Outcomes (1)
investigate and optimize imaging sequences and parameters of rapid real-time MRI in order to obtain adequate guidance for accurately and precisely delivering radiation to moving abdominal and thoracic tumors.
two hours
Interventions
Eligibility Criteria
Eligible disease(s)/stage(s) \\AJCC Stage I, II, III or IV lung, liver or pancreatic cancer of any histology to be treated using radiotherapy will be eligible for this study.
You may qualify if:
- Allowable type and amount of prior therapy \ Any types and amounts of prior therapy will be allowed for this study.
- Age restriction and/or gender/ethnic restrictions \\Patients must be greater than or equal to 18 years of age. There are no gender or ethnic restrictions.
- Life expectancy restrictions \ None.
- ECOG or Karnofsky Performance Status \ Karnofsky performance status of 50 or greater
- Requirements for organ and marrow function \ None.
- Ability to understand and the willingness to sign a written informed consent document.
You may not qualify if:
- Metallic implants, embedded metallic objects, implanted biomedical devices e.g., cardiac pacemakers
- Women who are pregnant or trying to get pregnant
- Pain in supine position
- Karnofsky performance status \< 50
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Stanford University School of Medicine
Stanford, California, 94305, United States
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Amit Sawant
Stanford University
- PRINCIPAL INVESTIGATOR
Paul J Keall
Stanford University
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 16, 2009
First Posted
February 19, 2010
Study Start
February 1, 2009
Primary Completion
September 1, 2010
Study Completion
September 1, 2010
Last Updated
December 7, 2012
Record last verified: 2012-12