Viewing Study NCT02894632


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Study NCT ID: NCT02894632
Status: COMPLETED
Last Update Posted: 2016-09-09
First Post: 2016-08-24
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: MR Compatible Accelerometer for Respiratory MOTion Measurement
Sponsor: Central Hospital, Nancy, France
Organization:

Study Overview

Official Title: MR Compatible Accelerometer for Respiratory MOTion Measurement
Status: COMPLETED
Status Verified Date: 2016-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: MARMOT
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.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: