Evaluation of NMES for Reducing Pain and Improving Functional Outcomes in Knee OA Patients

CyMedica Orthopedics

Status

Completed

Conditions

Knee Arthritis

Knee Pain Chronic

Knee Osteoarthritis

Treatments

Device: Active NMES

Study type

Interventional

Funder types

Industry

Identifiers

NCT03980964

CY-0030-306

Details and patient eligibility

About

The present prospective trial is designed to evaluate the efficacy of CyMedica Orthopedics e-vive™ system, a multifunctional electrotherapy device providing neuromuscular electrical stimulation (NMES) for reducing pain and accelerating functional recovery in patients with knee osteoarthritis. This post-market trial will involve patients who have been diagnosed with knee osteoarthritis, Kelgren-Lawrence Grades II, III, and IV. It is hypothesized that the use of the CyMedica e-vive NMES can reduce pain, improve knee function, and improve quality of life.

Full description

The study will be conducted at Lenox Hill Hospital, Northwell Health, located in New York, New York, and involve a total of 120 patients. All study patients will be evenly divided into two groups: (a) conductive garment and mobile app with NMES therapy; (b) conductive garment and mobile app without NMES therapy (sham).

Eligible patients will be evaluated according to the time and events schedule. Clinical outcomes will be assessed from 1 to 10 days before day of intervention and followed up after intervention over a 24 weeks ± 1 week study period.

These two groups will be analyzed using several outcome measures including validated patient-reported outcome measures including Visual Analogue Scale (VAS) pain level, the Knee Injury and Osteoarthritis Outcome Score (KOOS) JR., KOOS ADL, and WOMAC survey. Functional measures include isometric quadriceps strength, Time Up and Go (TUG), 6 minute walk test, repeated chair rise test, stair climb test, and number of steps recorded by an Apple Watch Series 3 or a Samsung watch. Reduction of use of anti-inflammatory medications (NSAIDS) and narcotics, use of ambulation assist devices, plan for TKA procedure survey, device compliance use, and patient satisfaction survey will be tracked The primary endpoint for the study is Visual Analogue Scale (VAS) pain The proprietary app for this product will be used to track device usage (intensity, duration of session, frequency of use), VAS, WOMAC, and KOOS JR.

Enrollment

40 patients

Sex

All

Ages

18 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Patients with symptomatic Kellgren-Lawrence (KL) Grade 2, 3, or 4 OA by radiograph (AP tunnel view) within 30 days prior to day 0 visit, where the K-L grades are defined as:
- Grade 0: no radiographic features of OA are present
- Grade 1: doubtful joint space narrowing (JSN) and possible osteophytic lipping
- Grade 2: definite osteophytes and possible JSN on anteroposterior weight-bearing radiograph
- Grade 3: multiple osteophytes, definite JSN, sclerosis, possible bony deformity
- Grade 4: large osteophytes, marked JSN, severe sclerosis and definite bony deformity
Patients who are between the ages of 18 - 85 years
Patient has signed informed consent
Patient has access to a smartphone or tablet (Android or iOS)
Subject must be ambulatory.
Subject must be willing to stop taking any pain medications 24 hours prior any scheduled study visit.
Subjects must be proficient in English.
Subject must be willing and able to sign an informed consent document.
Subjects must be willing and able to comply with all study procedures for the duration of the clinical study.

Exclusion criteria

Subjects who have a body mass index > 40 at the time of consent. Exclusion of a patient with BMI>40 is up to the discretion of the PI.
Subjects with a diagnosis of inflammatory arthritis (rheumatoid arthritis, gout, joint infection, Lyme disease, SLE, etc.).
Subjects who have had an injury or an acute traumatic injury to the index knee within 6 months of screening will be excluded.
Subject must NOT have had arthroscopy within 8 weeks of randomization.
Subjects who have had treatment of the target knee with intra-articular injections of steroids within 8 weeks of screening.
Subjects who have had intra-articular injections of hyaluronic acid within 12 weeks of screening.
Subjects who have had a scheduled surgery on the target knee within the study period.

(Note- Patients who are scheduled to go under surgery within the next 6 months will be excluded. Patients that are contemplating the surgery can be included.)
Subjects who have used electrotherapy or acupuncture for OA of the target knee within 4 weeks of screening
Subjects with significant and clinically evident mal-alignment of the target knee (> 10 degrees varus or valgus in the target knee).
Subjects with surgical metallic hardware in the target knee.
Subjects who have contraindications to MRI and X-rays, for example, implanted electrical devices (cardiac pacemakers, deep brain stimulators).
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.
Subjects who have an active substance abuse problem (drugs or alcohol) or a history of chronic substance abuse (> 5 years).
Subjects with skin breakdown or infection in the area where the study device will be placed.
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.
Subjects who have any ongoing litigation for worker's compensation.
Subjects with any condition, in the opinion of the Investigator that might interfere with the evaluation of the study objectives.
Subjects who are pregnant.
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