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Medical Device for Magnetic Therapy for Spinal Cord Injuries (SCI)

Medical Device for Magnetic Therapy for Spinal Cord Injuries (SCIMAG)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02333695
Acronym
SCIMAG
Enrollment
50
Registered
2015-01-07
Start date
2015-01-31
Completion date
2015-08-31
Last updated
2015-01-07

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

Conditions

Spinal Cord Injury, Stroke

Keywords

SCI, Spinal Cord Injury, Stroke

Brief summary

A medical device for magnetic therapy for spinal cord injuries (SCI) will be disclosed. The apparatus comprises a combination of several magnets enclosed in a supportive cover. The magnets are placed in a proper position and their polarity can be changed at any time without any difficulty.

Detailed description

A medical device for magnetic therapy for spinal cord injuries (SCI) will be disclosed. The apparatus comprises a combination of several magnets enclosed in a supportive cover. The magnets are placed in a proper position and their polarity can be changed at any time without any difficulty. The device provides a source of stimulation for the nerve to achieve therapeutic results and rehabilitation of patients with spinal trauma or stroke. A spinal cord injury - damage to any part of the spinal cord or nerves at the end of the spinal canal - often causes permanent changes in strength, sensation and other body functions below the site of the injury. Many scientists are optimistic that advances in research will someday make the repair of spinal cord injuries possible. Research studies are ongoing around the world. In the meantime, treatments and rehabilitation allow many people with a spinal cord injury to lead productive, independent lives. The effects of SCI depend on the type of injury and the level of the injury. SCI can be divided into two types of injury - complete and incomplete. Complete: A complete injury means that there is no function below the level of the injury; no sensation and no voluntary movement. Both sides of the body are equally affected. Incomplete: An incomplete injury means that there is some functioning below the primary level of the injury. A person with an incomplete injury may be able to move one limb more than another, may be able to feel parts of the body that cannot be moved, or may have more functioning on one side of the body than the other. With the advances in acute treatment of SCI, incomplete injuries are becoming more common. Spinal Magnetic Stimulation (SMS) is a relatively new way to use magnetism to affect the spinal cord. It is non-invasive, meaning that the procedure does not require any type of surgery; rather, it is conducted by transmitting magnetic pulses through the Spinal Cord by pressing a machine against the back. The Long term goal of this research project is the implementation of an effective, inexpensive therapy in patients with spinal cord injury. Another objective is the development of a cheap, presentable and comfortable magnetic device that causes neural stimulation to stop and reversing the signs and symptoms of Spinal Cord injury. The short-term objective is to prove that magneto stimulation is an intervention that reverses the signs and symptoms of Spinal Cord injury in an early and moderate State

Interventions

Spinal Magnetic Stimulation (SMS) is a relatively new way to use magnetism to affect the spinal cord. It is non-invasive, meaning that the procedure does not require any type of surgery; rather, it is conducted by transmitting magnetic pulses through the Spinal Cord by pressing a machine against the back.

Sponsors

American Society Of Thermalism And Climatology Inc
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* informed consent; * persons with confirmed and verified lesion of the central nervous system

Exclusion criteria

* Identification of the study a total intolerance to a pulsed magnetic field; * Development after inclusion of acute myocardial infarction and acute ischemic; * Installation of the pacemaker, intracardiac catheters or operations on the brain, requiring the abandonment of metal objects in the cranial cavity; * Pregnancy; * Enhancement of the patient, which requires the maintenance of vital functions by hardware (mechanical ventilation, continuous application infusomats); * The emergence of an epileptic seizure ; * Failure of the patient to continue participation in the study;

Design outcomes

Primary

MeasureTime frame
Reduction Hiperrelexia30 days

Secondary

MeasureTime frame
Stimulate an erection45 days
Stimulate bowel movements30 days
Stimulate bladder emptying30 days

Other

MeasureTime frame
Reduce muscle spasticity following upper motor neuron lesions45 days
Induce cough to prevent respirator infections.45 days

Countries

United States

Contacts

Primary ContactGaris Silega, MD
drsilega@aol.com9738426230

Outcome results

None listed

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