Efficacy and Safety of an Active Pulsed Electromagnetic Field for the Treatment of Osteoarthritis of the Knee

The hypothesis of this study is that exposure to PEMF alters the cytokine environment of OA
joints associated with a reduction of inflammation and improved homeostasis of the
extracellular matrix (ECM), both potentially effecting symptomatic relief of OA pain,
reducing cartilage breakdown, stimulate new cartilage formation therefore preserving joint
structure. The primary objective of this study is to prospectively determine, at 12 months
post treatment, the safety and efficacy of treating OA of the knee with PEMF. Safety will be
assessed through adverse event collection. Study subjects will be randomized in a 2:1 ratio
(active: placebo control) to either an active or placebo control (inactive) Physio-Stim
device. The study is powered to detect a significant difference between groups when 120
subjects (80 active: 40 placebo control) have completed the study. Planned enrollment for the
study is 150 subjects, to allow for an attrition rate of 20%.

Inclusion Criteria:

1. Subject must be able to wear the investigational device so that there is adequate PEMF
exposure to the knee.

2. Subject must have a body mass index ≤ 45 at the time of consent.

3. Subject must be at least forty (≥ 40) years of age of age at the time of consent.

4. Subject must have an established diagnosis of primary femorotibial OA in the target
knee by modified American College of Rheumatology criteria for at least 6 months and
at least one of the following:

i. Stiffness less than 30 min ii. Crepitus (noise or cracking on knee motion)

5. Subject must have symptomatic Kellgren-Lawrence (K-L) Grades 1-3 OA by radiograph (PA
flexion) within 90 days of screening, where the K-L grades are defined as:

Grade 1: doubtful narrowing of joint space and possible osteophytic lipping; Grade 2:
definite osteophytes and definite narrowing of joint space; Grade 3: moderate multiple
osteophytes and definite narrowing of joint space and some sclerosis and possible
deformity of bone contour

6. Subject must have a visual analog pain score between 4 cm and 8 cm on a 10 cm scale in
the target knee at the time of screening.

7. Subject must have a normal tibiofemoral angle (0-8°) and a joint space width of ≥ 3mm
confirmed by radiograph.

8. Subject must be ambulatory.

9. Subject must NOT have had arthroscopy within 8 weeks of randomization.

10. Subject must NOT have had viscosupplementation within 8 weeks of randomization.

11. Subject must NOT have had NSAIDs within 1 week of randomization (low-dose aspirin as
cardioprotective prophylaxis is permitted).

12. Subject must be willing to discontinue corticosteroids administered by any route
except intranasal spray, steroid- containing ophthalmic solutions and anti-asthmatics.

13. Subject must be willing to take acetaminophen (up to 3000 mg/day) as pain medication
for the duration of the study. Other pain medications may be allowed during the course
of the study if the subject meets specific criteria.

14. Subject must be willing to STOP taking any pain medications 24 hours prior any
scheduled study visit.

15. Subject must NOT have participated in a clinical study within the past 12 weeks that
required the use of an investigational device, drug or biologic.

16. Subjects must be proficient in English.

17. Subject must be willing and able to sign an informed consent document.

18. Subjects must be willing and able to comply with all study procedures for the duration
of the clinical study.

Exclusion criteria:

1. Subjects who have a body mass index > 45 at the time of consent.

2. Subjects with a diagnosis of inflammatory arthritis (rheumatoid arthritis, gout, joint
infection, Lyme disease, SLE, etc.).

3. Subjects with a diagnosis of secondary arthritis (acromegaly, Charcot's arthropathy,
hemochromatosis, Wilson's disease, ochronosis, etc.).

4. Subjects with confounding factors such as ipsilateral hip OA or chronic pain syndromes
(fibromyalgia, Crohn's disease, ulcerative colitis, interstitial cystitis).

5. Subjects who have had an injury or an acute traumatic injury to the index knee within
6 months of screening will be excluded.

6. Subjects who have had treatment of the target knee with intra-articular injections of
steroids within 8 weeks of screening.

7. Subjects who have had intra-articular injections of hyaluronic acid within 8 weeks of
screening.

8. Subjects who plan to have surgery on the target knee within the study period.

9. Subjects who have used electrotherapy or acupuncture for OA of the target knee within
4 weeks of screening.

10. Subjects with significant and clinically evident mal-alignment of the target knee (>
10 degrees varus or valgus in the target knee).

11. Subjects with surgical metallic hardware in the target knee.

12. Subjects with pain in any other area of the lower extremities or back that is equal to
or greater than the pain in the target knee.

13. Subjects who have contraindications to MRI and X-rays, for example, implanted
electrical devices (cardiac pacemakers, deep brain stimulators).

14. Subjects with a current malignancy or who have received treatment for malignancy with
the last 5 years, with the exception of resected basal cell carcinoma and squamous
cell carcinoma of the skin.

15. Subjects who have an active substance abuse problem (drugs or alcohol) or a history of
chronic substance abuse (> 5 years).

16. Subjects with skin breakdown or infection in the area where the study device will be
placed.

17. Subjects with any chronic conditions (e.g., diabetes, hypertension, congestive heart
failure, etc.) that have not been well-controlled for at least 3 months prior to
screening.

18. Subjects who have any ongoing litigation for worker's compensation.

19. Subjects with any condition, in the opinion of the Investigator that might interfere
with the evaluation of the study objectives.

20. Subjects who are unwilling or unable to adhere to the follow up schedule and
procedures.

21. Subjects who are pregnant.

22. Subjects who are prisoners.