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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02333695
Other study ID # Gavionerrvemag
Secondary ID
Status Recruiting
Phase N/A
First received January 5, 2015
Last updated January 6, 2015
Start date January 2015
Est. completion date August 2015

Study information

Verified date January 2015
Source American Society Of Thermalism And Climatology Inc
Contact Garis Silega, MD
Phone 9738426230
Email drsilega@aol.com
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial 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.


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


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date August 2015
Est. primary completion date August 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility 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;

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Spinal Magnetic Stimulation
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.

Locations

Country Name City State
United States Gaviota Clinic Newark New Jersey

Sponsors (1)

Lead Sponsor Collaborator
American Society Of Thermalism And Climatology Inc

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Reduce muscle spasticity following upper motor neuron lesions 45 days No
Other Induce cough to prevent respirator infections. 45 days Yes
Primary Reduction Hiperrelexia 30 days Yes
Secondary Stimulate an erection 45 days Yes
Secondary Stimulate bowel movements 30 days Yes
Secondary Stimulate bladder emptying 30 days Yes
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