An Investigation of ReNu™ Knee Injection in Patients With Osteoarthritis

NuTech Medical

Status: Completed

Conditions: Osteoarthritis

Treatments: Device: placebo saline; Procedure: Knee injection; Device: Hyaluronic Acid; Other: ReNu amniotic allograft

Study type: Interventional

Funder types: Industry

Identifiers

NCT02318511

RD2014-10-04

Details and patient eligibility

About

This is a Prospective, Randomized study evaluating the efficacy of ReNu for the treatment of Kellgren-Lawrence grade 2 or 3 osteoarthritis. Patients will be randomized into 1 of 3 groups for injection into the effected knee: 1) ReNu - study treatment, 2) Hyaluronic Acid (HA) injection - with commonly used injection material and 3) Saline. After treatment, patients will be followed up to 12 months to evaluate improvements using common pain and function subscales.

Enrollment: 200 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Patients with moderate knee osteoarthritis determined by a combination of clinical and radiographic findings and documented by Kellgren-Lawrence radiographic classification (Grade 2 or 3)
• Grade 2 Kellgren-Lawrence radiographic changes are defined as small osteophytes, possible narrowing of joint space
• Grade 3 Kellgren-Lawrence radiographic changes are defined as moderate multiple osteophytes, definite narrowing of joints space, some sclerosis and possible deformity of bone contour.
• Patients with bilateral grade 2 or 3 Kellgren Lawrence knee osteoarthritis who have bilateral symptoms may have their more symptomatic knee injected. If equivalent symptoms are reported by the patient, then the patient will choose which knee is to be injected. The contralateral knee can be treated with local standard of care such as steroid injection, cold therapy or soft brace.
• Age 18 and older
• BMI less than 40
• 7 day average pain score of 4 or greater for the involved knee on a numeric pain scale from 1 to 10.
• Female patients must be actively practicing a contraception method, abstinence, be surgically sterilized, or be postmenopausal

Exclusion criteria

• Pain medication (including nonsteroidal antiinflammatory drugs, NSAIDs) less than 15 days before injection (may take acetaminophen)
• Receiving pain medication other than acetaminophen for conditions unrelated to osteoarthritis of the index knee
• Regular use of anticoagulants, such as Coumadin, dabigatran or rivaroxaban; use of antiplatelet medications are not a reason for exclusion
• History of substance abuse.
• Failure to agree NOT to take additional knee symptom modifying drugs, other than acetaminophen, during the course of the study without reporting to the study team
• Pregnancy or desire to become pregnant during study duration
• Positive pregnancy test on premenopausal subject
• Morbid obesity (defined as BMI 40 or greater)
• Symptoms of locking, intermittent block to range of motion or loose body sensation which could indicate meniscal displacement or an intraarticular loose body
• Corticosteroid injection into the index knee within 3 months
• Viscosupplement injection into the index knee within 3 months
• Knee surgery of involved index knee within 12 months
• Knee surgery contralateral knee 6 months
• Worker compensation
• Acute index knee injury (injury within 3 months)
• History of Diabetes mellitus
• History of solid organ or hematologic transplantation
• History of rheumatoid arthritis or other autoimmune disorder
• Diagnosis of a non-basal cell malignancy within the preceding 5 years
• Infection requiring antibiotic treatment within the preceding 3 months
• Current therapy with any immunosuppressive medication, including corticosteroids at a dose > 5 mg per day

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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200 participants in 3 patient groups, including a placebo group

ReNu amniotic allograft

Experimental group

Description:

Knee injection with ReNu. ReNu is an allograft tissue composed of particularized amniotic membrane and cell from the amniotic fluid.

Treatment:

Procedure: Knee injection

Other: ReNu amniotic allograft

Saline

Placebo Comparator group

Description:

Knee injection with saline. Injectable saline will be used as the placebo control.

Treatment:

Procedure: Knee injection

Device: placebo saline

HA injection

Active Comparator group

Description:

Knee injection with HA. HA will be used as a viscosupplementation injection consisting of cross linked HA.

Treatment:

Procedure: Knee injection

Device: Hyaluronic Acid