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Uncertainty Analysis of Computational Model to Simulate Neurostimulation Caused by Gradient Fields in MRI

Uncertainty Analysis of Computational Model to Simulate Neurostimulation Caused by Gradient Fields in MRI

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04674787
Acronym
NEUROMAN
Enrollment
12
Registered
2020-12-19
Start date
2021-03-01
Completion date
2021-03-20
Last updated
2021-05-26

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

Conditions

Electric Stimulation, Peripheral Nerve Stimulation in MRI

Keywords

MRI gradient coil, peripheral nerve stimulation, Time varying magnetic fields

Brief summary

The aim of this research project is to quantify the uncertainty of current state-of-the art anatomical phantoms and computational models for predicting neurostimulation induced by time-varying magnetic fields (so-called gradient fields) within the context of magnetic resonance imaging (MRI) scanners. For this purpose stimulation thresholds will be measured in a volunteer study. The measurements will provide valuable data for the development and validation of future models.

Detailed description

The study does not investigate any health related interventions, neither a therapy nor medical device. The study aims to provoke peripheral nerve stimulation from time varying magnetic (so-called gradient) fields in volunteers in order to measure gradient threshold levels in different configurations (different gradient coil units, different positions and postures). The experiments will provide new data regarding the interaction of gradient fields and function of the peripheral nervous system. These measurements are of general interest to quantify associated modeling uncertainties and validate current or future computational modeling techniques. The experiments will use an MR scanner to generate the gradient fields used to induce stimulation. In normal mode the maximum gradient field allowed by the manufacturer may lead to peripheral nerve stimulation in approximately 50% of subjects. However, depending on the position and posture it may induce PNS in even fewer than 50% of subjects. Therefore, for the purpose of measuring stimulation thresholds it is necessary to operate the gradient units in experimental mode (with respect to the gradient field) as described in IEC 60601-2-33, i.e. the gradient limits set by the manufacturer will be disabled. As described in the standard, the gradient field will be increased slowly from non-stimulating levels until the volunteer perceives first stimulation sensations, at which point the gradient field will be stopped. This protocol does not lead to an increased risk of cardiac muscle stimulation compared to the normal mode, but only an increased likelihood of PNS with non-painful sensations in the skin, e.g. tingling, twitching or poking. PNS is not considered a health concern. The radio-frequency (RF) field will remain switched off, i.e. there is no risk of heating (the scanner will not acquire images in this mode).

Interventions

OTHERPeripheral nerve stimulation provocation study

Study which measures stimulation thresholds in volunteers induced by low frequency electromagnetic gradients used in MRI scanners.

Sponsors

Institute for Biomedical Engineering, Swiss Federal Institute of Technology (ETH Zurich)
CollaboratorUNKNOWN
Bryn Lloyd
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* healthy adult volunteers (six female and six male)

Exclusion criteria

* pregnant woman * metallic implants or a history of neurological or cardiovascular diseases * children and persons who are not able to follow the instructions will be excluded, due to a higher risk and lack of direct benefits from participation

Design outcomes

Primary

MeasureTime frameDescription
Measure PNS stimulation thresholdsThe experimental procedure will be conducted during a single visit of approx. 90 minutes.The primary objective is to measure PNS stimulation thresholds in order to quantify the modeling uncertainty and reliability.

Countries

Switzerland

Outcome results

None listed

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