Investigation of Mesenchymal Stem Cell Therapy for the Treatment of Osteoarthritis of the Knee
September 23, 2019 updated by: Joseph Ruane, OhioHealth
Investigation of Mesenchymal Stem Cell Therapy for the Treatment of Osteoarthritis of the Knee: Effect on Pain and Quality of Life
The purpose of this study is to determine the clinical response to autologous bone marrow aspirate concentrate (BMAC) and platelet-rich plasma (PRP) injections for knee osteoarthritis with respect to pain, function, and quality of life at up to 1 year following the intervention.
Specifically, the clinical response will be compared to baseline and a control group treated with a Gel-One® hyaluronate injection to the target knee.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
32
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Ohio
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Columbus, Ohio, United States, 43214
- McConnell Spine, Sport, and Joint Physicians
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
36 years to 66 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Male and female patients 40 to 70 years old
- Diagnosed with knee osteoarthritis based on the American College of Rheumatology criteria including symptomatic reports and radiographic findings
- Kellgren-Lawrence grade 1-3 based on a radiograph within 6 months of presentation to the clinic
- Symptomatic evidence of tibiofemoral osteoarthritis for ≥6 months
- Average numeric pain rating of 4 - 8 on a scale of zero to 10 (defined as moderate level) over the past week
- Previous trial of 6 weeks minimum of conservative therapy including physical therapy, weight loss, anti-inflammatory medication, or injection therapy
Exclusion Criteria:
- Grade 4 knee osteoarthritis according to the Kellgren-Lawrence scale
- History of intraarticular viscosupplementation or steroid injection in the target knee in the past 6 months at the time of the baseline visit or intraarticular injection planned during the trial
- History of arthroscopic surgery in the target knee in the past 12 months at the time of presentation to the clinic or planned surgery during the trial period (e.g., scheduled for/awaiting arthroscopy or a knee replacement procedure)
- Bilateral knee osteoarthritis (unless the contralateral knee involvement is limited to radiographic osteoarthritis and not symptomatic)
- Ipsilateral (same side) or contralateral (opposite side) symptomatic osteoarthritis of hip or ankle
- Clinically apparent tense effusion or other acute inflammation of the target knee at the time of presentation to the clinic
- Active infection of either lower extremity such as cellulitis or any skin disease or infection in the area where BMAC is aspirated, blood is drawn, or an injection is given
- History of diagnosis of any of the following: 1) septic osteoarthritis of any joint, 2) inflammatory arthropathy such as rheumatoid arthritis, gout, pseudogout, lupus, crystalline arthropathy, chondrocalcinosis and other rheumatology diagnoses
- Cruciate/collateral knee ligament instability, ligament laxity, or meniscal instability of the target knee
- Significant alignment deformity such as varus/valgus of the target knee in the judgment of the investigator
- Currently pregnant, nursing, or planning to become pregnant during the trial period
- Previous or known allergic reaction or hypersensitivity to heparin; sodium citrate; hyaluronan products or specifically Gel-One®; cinnamon; bird products such as feathers, eggs, or poultry; avian proteins
- Not suitable for BMAC tissue allograft injection per physician (e.g., blood dyscrasia)
- Unable to be prescribed stable dose of NSAIDs and/or tramadol based on medical history as ad lib use of over-the-counter analgesics will be allowed in both groups after treatment
- Current cigarette smoker
- Unable to give informed consent
- Non-English speaking
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: BMAC injection and PRP injection
Injection of bone marrow aspirate concentrate (BMAC) withdrawn from a bone near the hip into the knee joint (intra-articular) immediately followed by an injection of platelet-rich plasma (PRP) into the knee joint.
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60mL of bone marrow will be collected from a bone near the hip.
Approximately 5-6mL of the bone marrow aspirate concentrate is then used for injection, under ultrasound guidance, into the target knee by the study physician.
60mL of venous blood will be withdrawn from either arm.
Approximately 4-5 ml of platelet-rich plasma will be introduced under ultrasound guidance to the subject's target knee by the study physician.
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Active Comparator: Gel-One® hyaluronate injection
Gel-One® is an hyaluronate gel used in the treatment of knee osteoarthritis by injection into the knee joint (intra-articular).
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Patients will receive a single injection of Gel-One® (3 ml syringe of Gel-One® - 1% solution [10 mg/mL], 30mg total hyaluronan) into the target knee.
Injections will be performed by the study physician under real-time dynamic ultrasound guidance.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Knee Injury and Osteoarthritis Outcome Score
Time Frame: Change from baseline to 3, 6, and 12 months post-treatment
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Subscales include pain, symptoms, function in activities of daily living, function in sport and recreation, and knee-related quality of life.
Each subscale is 0-100 with 100 indicating the best possible score.
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Change from baseline to 3, 6, and 12 months post-treatment
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Numeric Pain Rating Scale
Time Frame: Change from baseline to 3, 6, and 12 months post-treatment
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Scale from 0-10 with 0 representing "no pain" and 10 representing "worst imaginable pain"
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Change from baseline to 3, 6, and 12 months post-treatment
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Patient Reported Outcome Measurement Information System Global Health Scores
Time Frame: Change from baseline to 3, 6, and 12 months post-treatment
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The Patient Reported Outcomes Measurement Information System (PROMIS®) Global Health scale v1.1 contains 10 questions and produces two subscale scores: Global Physical Health (GPH) and Global Mental Health (GMH) (Hays, Bjorner, Revicki, Spritzer, & Cella, 2009).
Each subscale produces a raw score that is converted to a T score such that an average patient in the United States would have a subscale T score of 50 with a standard deviation of 10 points ("Global Health: A Brief Guide to the PROMIS® Global Health Instruments", 2017).
A score higher than the mean indicates a more desirable score, and vice versa.
A positive change score indicates an improvement, while a negative change score indicates a decline in score value.
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Change from baseline to 3, 6, and 12 months post-treatment
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Joseph J Ruane, DO, Medical Director, McConnell Heart Health Center
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2016
Primary Completion (Actual)
August 1, 2018
Study Completion (Actual)
August 1, 2018
Study Registration Dates
First Submitted
November 3, 2016
First Submitted That Met QC Criteria
November 4, 2016
First Posted (Estimate)
November 8, 2016
Study Record Updates
Last Update Posted (Actual)
September 24, 2019
Last Update Submitted That Met QC Criteria
September 23, 2019
Last Verified
September 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- OH1-16-00672
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.