Lower Extremity Swelling Acute
Conditions
Brief summary
Physician Clinical Trial Policy (CTP) to evaluate the efficacy treatment of lower extremity pathologies derived from neurological ischemia disorders using the combination of Monochromatic Infrared Photo Energy (MIRE) and Transcutaneous Electrical Nerve Stimulation (TENS) therapies.
Detailed description
Although there are a number of pain disorders, associated with back, or lower extremity pain and swelling, the American Association of Sensory Electrodiagnostic Medicine (AASEM/ DTSC) study programs will accumulate received data following a protocol of treatment performed for the purpose of eliminating pain, reducing swelling, and accelerating recovery periods as well as to record the success or failure and/or improvement of the malfunctioning body part. * Condition: Neuropathic Pain, Tingling or Numbness derived from neurological Ischemia * Intervention: Treatments of Monochromatic Infrared Photo Energy (MIRE) in combination with Electronic Signal Treatment (TENS) therapy * Study Type: Interventional * Study Design: 1. Allocation: Non-Randomized 2. Endpoint Classification: Efficacy Study 3. Intervention Model: Single Group Assignment 4. Masking: Open Label 5. Primary Purpose: Scientific record of treatment success or failure
Interventions
DEVICEAnodyne
Subjects will be treated with MIRE therapy using the Anodyne® device within 72 hours of previous treatments, and in accordance with the Anodyne® package insert indications for use 30 to 45 minutes professional units on power setting of 8,. In addition, patients will undergo TENS therapy with the use of either the Avazzia® Pro Sport or TENS 3000 (for no less than 30 mins, both on label) in accordance with the indications for use of each TENS device, for a minimum of 15 minutes at the subjective site for pain and each vertebrae nerve base, when impairment is confirmed with the objective Small Pain Fiber (SPF) Nerve Conduction Study (NCS) test performed.
Sponsors
American Association of Sensory Electrodiagnostic Medicine
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
25 Years to 90 Years
Healthy volunteers
No
Inclusion criteria
* In the investigator's judgment, a high probability of 5 year survival and compliance with the study visit schedule. Ability to comprehend and sign an informed consent document prior to study enrollment.
Exclusion criteria
* Any other excluding factors that, according to the investigator's judgment, would preclude enrollment in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary Outcome: Scientific record of treatment success or failure | 5 years |
Outcome results
None listed