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MR Compatible Accelerometer for Respiratory MOTion Measurement

MR Compatible Accelerometer for Respiratory MOTion Measurement

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02894632
Acronym
MARMOT
Enrollment
24
Registered
2016-09-09
Start date
2013-07-31
Completion date
2016-08-31
Last updated
2016-09-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Disease

Keywords

MRI, Motion, Respiratory movement, Artifacts correction

Brief summary

A novel magnetic resonance (MR) compatible accelerometer for respiratory motion sensing (MARMOT) has been developed as a surrogate of the vendors' pneumatic belts. The aim is to model and correct respiratory motion for free-breathing thoracic-abdominal MR imaging and to simplify patient installation.

Detailed description

Respiratory motion is a serious problem in the acquisition of high-quality thoracic/abdominal magnetic resonance (MR) images. Various methods have been proposed to compensate the motion-induced artefacts, including breathholding, respiratory gating and model-driven motion correction. Breath-holding is the simplest among the three. However this conventional clinical method induces various problem, including inefficient use of scanners, inconsistent organ position between each breath-hold, imaging an altered physiological status and patient inconvenience especially for those who suffer from respiration difficulties. Free-breathing MR acquisition has therefore become of great clinical interest recently. The investigators intend to examine the efficacy of the MARMOT sensors for: * modelling and predicting the respiratory motions in abdominal scans, * correcting for the respiratory motion in a cardiac cine scan, via a reconstruction-based method.

Interventions

DEVICEMRI compatible motion sensor (MARMOT)

MRI with motion control (several motion sensors placed on the volunteer's body)

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* To not have cardiac, hepatic or renal pathology * To be more than 18 * To be enrolled in a social security plan * To have signed an informed consent * To have preliminary medical examination

Exclusion criteria

* Contraindication: implantable devices (pacemakers, defibrillators, cochlear implants, etc.), metallic foreign bodies * Impossibility to undergo MRI : claustrophobia, morbid obesity * Pregnancy or risk of pregnancy * Patient under a measure of legal protection

Design outcomes

Primary

MeasureTime frameDescription
Respiratory movement using respiratory beltsfour monthsRespiratory belts, which are usually used in MRI to monitor respiratory movements and brath-holding, are placed around the volunteer's body (on the abdominal and on the thoracic level). They give the average displacement (in mm) across time generated by the respiratory movement.
Respiratory movement using MARMOT sensorsfour monthsMARMOT sensors are placed on the volunteer's body (4 sensors placed on the thorax or on the abdomen). MARMOT sensors give 2 measures : acceleration generated by the respiratory movement (in mm/s²) in 3 directions and rotation generated by the respiratory movement (angle in °/s) in 3 directions.
Respiratory movement using real-time MR imagesfour monthsMotion measurement (in mm) directly on the MR images (using real-time MR imaging)

Secondary

MeasureTime frameDescription
Subjective quality (marks between 1 (the best) and 3 (the worst) of the reconstructed MR images)four monthsComparing the quality of the reconstructed cardiac cine images obtained with the cine-GRICS algorithm using: * the pneumatic belts alone * all MARMOT signals * signals from only one MARMOT sensor. Three cardiologists are shown with the motion-compensated cine movies obtained using these three sensor configurations. The movies are presented in random ordering on the screen so that the clinicians are blind to the sensor configuration. They are then asked to rank them by overall image quality (1=best, 2=second best, 3=worst). Equal quality ranking is allowed in this procedure.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026