CClinicalTrials.gg
CompletedNCT01632800Updated Oct 8, 2019Results posted

Sensory Effects of Rapidly-Changing Magnetic Fields

An interventional study of High pulsed magnetic fields in Sensory Disorders, sponsored by Weinberg Medical Physics LLC. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-10-08.

Sponsored by Weinberg Medical Physics LLC · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
26
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

This study is being conducted to improve magnetic resonance imaging (MRI) scans by reducing the time required for imaging. Experience has shown that unpleasant side-effects from magnetic pulses used in MRI (for example, tingling or tapping sensations) can be reduced when the magnetic pulses are shortened. In this study, we will explore whether this effect holds true when very short magnetic pulses are applied.

Read the detailed description

See above

02

Conditions studied

  • Sensory Disorders

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Keywords

  • Magnetic fields discomfort
03

In context

Sensation Disorders

73 studies on the registry are indexed under Sensation Disorders; 23 are open to participants now.

This study's enrollment of 26 is below the median of 40 across 45 interventional studies indexed under Sensation Disorders.

Browse Sensation Disorders studies →

Lead sponsor

Weinberg Medical Physics LLC is the lead sponsor of 3 studies on the registry; 1 is open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Adults over 18, capable of informed consent

Exclusion criteria

Exclusion Criteria:

  • History of arrhythmia. Has implanted pacemaker or defibrillator, right wrist-to-sternum distance of less than 60 centimeters, visible tattoos of the right hand or wrist, or with any metallic objects that cannot be removed from the right hand or wrist. Irregular or imperceptible pulse. Heart rate less than 50 beats per minute or more than 100 per minute, resting respiratory rate greater than 25 per minute, diastolic blood pressure less than 50. Solid meal ingested within 2 hours prior to the study.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
26 participants (actual)

Study arms

  • Experimental
    Single arm study

    Each subjects will undergo escalating exposure to magnetic field

    Device: High pulsed magnetic fields

Interventions

  • DeviceHigh pulsed magnetic fields

    Magnetic fields will escalate in strength

    Also known as: Pulser is custom built by Applied Pulsed Power, Ithaca NY

06

What researchers measure

Primary outcomes

  1. Degree of Discomfort Under Applied Pulsed Magnetic Fields

    Pulsed magnetic fields will be applied a total of forty-eight times to the right hand of each subject. After each time the magnet coil is pulsed, the subject will be asked if he or she notices any sensation (for example, tingling or tapping). Subjects will be asked to rate the sensation from 0 to 4, where 0 means no sensation, 1 means barely-noticeable sensation, 2 means easily noticeable sensation, 3 means unpleasant sensation, and 4 means very unpleasant sensation.

    Time frame: Bioeffects will be assessed within the five-minute application of each pulse sequence

07

Results

Posted Jun 15, 2016

Participant flow

Participant flow — Overall Study
MilestoneSingle Arm Study
Started26
Completed25
Not completed1
Withdrew: Subject did not fit in apparatus1

Outcome measures

PrimaryDegree of Discomfort Under Applied Pulsed Magnetic Fields

Pulsed magnetic fields will be applied a total of forty-eight times to the right hand of each subject. After each time the magnet coil is pulsed, the subject will be asked if he or she notices any sensation (for example, tingling or tapping). Subjects will be asked to rate the sensation from 0 to 4, where 0 means no sensation, 1 means barely-noticeable sensation, 2 means easily noticeable sensation, 3 means unpleasant sensation, and 4 means very unpleasant sensation.

Time frame:
Bioeffects will be assessed within the five-minute application of each pulse sequence
Reported as:
Number · percentage of subjects with discomfort
Degree of Discomfort Under Applied Pulsed Magnetic Fields
percentage of subjects with discomfortSingle Arm Study
Degree of Discomfort Under Applied Pulsed Magnetic Fields0

Adverse events

Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Single Arm Study—0/25 (0%)0/25 (0%)

Baseline characteristics

Age, Continuous
Age, Continuous(years)Single Arm Study
Mean40.4 ± 16.8
Sex: Female, Male
Sex: Female, Male(Participants)Single Arm Study
Female14
Male11
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Single Arm Study
Hispanic or Latino0
Not Hispanic or Latino25
Unknown or Not Reported0
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Single Arm Study
American Indian or Alaska Native0
Asian1
Native Hawaiian or Other Pacific Islander0
Black or African American0
White24
More than one race0
Unknown or Not Reported0
Region of Enrollment
Region of Enrollment(participants)Single Arm Study
United States25
08

Study locations

1 site
  • Applied Pulsed Power
    Freeville, New York 13068, United States
09

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 8, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT01632800
Lead sponsor
Weinberg Medical Physics LLC
Collaborators
National Heart, Lung, and Blood Institute (NHLBI), National Institute of Neurological Disorders and Stroke (NINDS)
Responsible party
Sponsor
First posted
Jul 3, 2012
Start date
Aug 2011
Primary completion
Oct 2011
Completion
Oct 2011
Results posted
Jun 15, 2016
Last update
Oct 8, 2019

Study contacts

Stanley Fricke, PhD
principal investigator · Children's National Research Institute

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2019. You cannot join it, but the record below documents what was studied.

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