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CompletedNCT02019199Updated Jul 11, 2017

Magnetic Resonance Imaging (MRI) in Motion

An observational study in Liver Cancer, Lung Cancer, Pancreatic Cancer, sponsored by Duke University. Completed at 1 site in United States. Open to participants aged 21 Years and older. Per ClinicalTrials.gov, last updated 2017-07-11.

Sponsored by Duke University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
25
Ages
21 Years and older
Sex
All
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Study summary

This study is a research initiative established to explore the use of magnetic resonance imaging (MRI) as a tool for detecting organ motion as it pertains to planning radiation therapy.

Read the detailed description

The goal with radiation therapy is to treat the defined tumor and spare the surrounding normal tissue from receiving dose above specified tolerance doses. There is evidence of improved local control and survival with higher doses of radiation, however, at the same time there is the need to spare normal tissues from higher doses of radiation. Technologies that allow the delivery of an increased radiation dose to the tumor while sparing normal tissue have the potential of improving the therapeutic ratio. However, the development of these technologies has been hampered by organ respiratory motion particularly in the case of the lungs and liver. Inadequate radiation coverage of a tumor secondary to organ motion can lead to delivering a lower dose to a portion of the tumor. Making the field of radiation larger to account for organ motion results in unnecessary radiation dose to surrounding healthy tissues. It is therefore desirable to document the extent of motion of the organ in question prior to carrying out the radiation treatment planning. The organ motion impacts directly on the radiation dose distribution in the treatment volume.

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Conditions studied

  • Liver Cancer, Lung Cancer, Pancreatic Cancer
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In context

Pancreatic Neoplasms

3,235 studies on the registry are indexed under Pancreatic Neoplasms; 899 are open to participants now.

This study's enrollment of 25 is below the median of 200 across 620 observational studies indexed under Pancreatic Neoplasms.

Browse Pancreatic Neoplasms studies →

Lead sponsor

Duke University is the lead sponsor of 2,025 studies on the registry; 275 are open to participants now.

Of its 194 completed or terminated interventional studies of FDA-regulated products, 159 (82%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
21 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adults males or females with primary or secondary cancer tumors of the lung, liver or pancreas

Inclusion criteria

  • Age ≥ 21
  • Patients with primary or metastatic tumors in the lungs, liver, or pancreas
  • Patients undergoing a planning CT scan in the Department of Radiation Oncology with tumor motion assessment - planning 4D-CT ordered by the treating Radiation Oncologist
  • Signed, specific informed consent prior to study entry

Exclusion criteria

Exclusion Criteria:

  • Any condition for which a MRI procedure is contraindicated including presence of metallic material in the body, such as pacemakers, non- MRI compatible surgical clips, shrapnel, etc
  • Pregnant or breast-feeding women
  • Subjects who have difficulty lying flat on their back for extended periods of time
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
25 participants (actual)
Patient registry
No
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What researchers measure

Primary outcomes

  1. To evaluate the accuracy, robustness, and efficacy of MRI for tumor motion measurement.

    MRI and CT ( all subjects will have a standard of care CT scan) data in DICOM format will be collected for analysis using commercial or customized - developed software. Image quality will be assessed based on signal-to-noise (SNR), contrast-to-noise ratio (CNR), and the presence of image artifacts. Data to be computed include, but are not limited to, tumor volumes (gross tumor volume, internal target volume, planning target volume, etc.), tumor motion parameters (range, trajectory, frequency, variation, probability distribution, etc.), and treatment plan parameters (target coverage, dose-volume-histogram, etc.).

    Time frame: During MRI approx 1 hour

  2. Tumor volume

    Free breathing/breath-hold MRI will be compared to free breathing/breath-hold CT

    Time frame: During MRI approx 1 hour

  3. Tumor contrast-to-noise ratio (CNR)

    Difference between CNR is measured by 4D-MRI and 4D-CT

    Time frame: During MRI approx 1 hour

  4. Tumor Motion

    Difference between tumor motion as measured by 2D cine-MRI vs 4D-MRI vs 4D-CT

    Time frame: During MRI approx 1 hour

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Study locations

1 site
  • Duke University Medical Center
    Durham, North Carolina 27710, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 11, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02019199
Lead sponsor
Duke University
Responsible party
Sponsor
First posted
Dec 24, 2013
Start date
Nov 2011
Primary completion
Aug 2015
Completion
Aug 2015
Last update
Jul 11, 2017

Study contacts

Brian Czito, MD
principal investigator · Duke University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2017. You cannot join it, but the record below documents what was studied.

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