Stem Cell Study in Osteoarthritis of the Knee and Hip Joints
Study Details
Study Description
Brief Summary
The purpose of this trial is to compare the effect of a single intra-articular injection of Lipoaspirate Concentrate vs Bone Marrow Aspirate on pain reduction and functional improvement in the treatment of the knee and hip OA.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Detailed Description
The primary objective is to compare of magnitude and duration of pain relief of intra-articular injections with Lipoaspirate Concentrate vs Bone Marrow Aspirate.
The secondary objective is to compare the effect of Lipoaspirate Concentrate vs Bone Marrow Aspirate intra-articular injections on functional improvement, stiffness, global impression of change, and consumption of analgesic medication.
The exploratory objective is to explore the safety and the general tolerability of a single intra-articular injection of Lipoaspirate Concentrate vs Bone Marrow Aspirate.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: Knee arm randomized to Lipoaspirate Concentrate and Bone Marrow Aspirate The Subjects will be randomized to one of the treatment groups separately for the knee and hip arms of the study. Group A will receive a single intra-articular injection with lipoaspirate concentrate to the knee and Group B will receive a single intra-articular injection with bone marrow aspirate concentrate. |
Biological: Bone Marrow Aspirate, Lipoaspirate Concentrate
Autologous Cell Therapy.
|
| Active Comparator: Hip Arm randomized to Lipoaspirate Concentrate and Bone Marrow Aspirate The subjects will be randomized to one of the treatment groups separately for the knee and hip arms of the study. Groups C will receive a single intra-articular injection with lipoaspirate concentrate to the hip and Group D will receive a single intra-articular injection with bone marrow aspirate. |
Biological: Bone Marrow Aspirate, Lipoaspirate Concentrate
Autologous Cell Therapy.
|
Outcome Measures
Primary Outcome Measures
- The primary endpoint is the change from the Baseline to the Day 360 in WOMAC pain subscale pain subscale [360 days]
Secondary Outcome Measures
- Change from Baseline to Days 90, 180 in WOMAC pain subscale [90, 180 days]
- Change from Baseline to Days 90, 180, and 360 in WOMAC stiffness subscale [90, 180, 360 days]
- Change from Baseline to Days 90, 180, and 360 in WOMAC function subscale [90, 180, 360 days]
- Change from Baseline to Days 90, 180, and 360 in total WOMAC score [90, 180, 360 days]
- Change from Baseline to Days 90, 180, and 360 in Patient's Global Impression of Changes (PGIC) [90, 180, 360 days]
- Change in average weekly consumption of analgesic medications from Baseline to Day 90, 180, and 360 [90, 180, 360 days]
Eligibility Criteria
Criteria
Inclusion Criteria:
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Male or female, aged 18 to 95 years old
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Residents of Canada
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Written informed consent to participate in the study
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Willingness and ability to comply with the study procedures and phone visit schedules and ability to follow verbal and written instruction
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The NRS for at least 5 daily measures will be used to calculate the average score. An average NRS pain score 4-9 (moderate to severe pain).
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Diagnosis of symptomatic knee or hip osteoarthritis for at least 12 weeks prior to screening based on an X-ray performed within 1 year prior to screening period.
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Radiographic evidence of OA of the index knee or hip (Kellgren-Lawrence Grade I to IV) within 1 year prior to screening or during the screening period.
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Failed conservative treatment for more than 12 weeks before the screening, meaning that pain persists for more than 12 weeks after the patient tried two or more of the following medication or intervention in that period.
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oral analgesics, including over the counter medications and supplements,
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physiotherapy
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acupuncture
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bracing
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cortisone injections,
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hyaluronic acid injections,
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dextrose injections (prolotherapy)
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platelet-rich plasma injections
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Women of childbearing potential must use an effective method of contraception from 14 days prior to baseline visit to 360 days after intervention. Effective birth control considered for this trial are total abstinence; consistent use of birth control pills; injectable birth control methods; intrauterine device placement; and tubal ligation or male partner with vasectomy; diaphragm with contraceptive jelly or condom with contraceptive foam.
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Body mass index (BMI) ≤ 50 kg/m2
Exclusion Criteria:
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Women who are pregnant or planning to become pregnant during the trial period.
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Women of childbearing potential (not surgically sterile or post-menopausal for at least one year) not using a highly effective method of contraception such as total abstinence; consistent use of birth control pills; injectable birth control methods; intrauterine device placement; and tubal ligation or male partner with vasectomy; diaphragm with contraceptive jelly or condom with contraceptive foam.
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History of malignancy except for the diagnosis of basal cell carcinoma > 5 years prior to the study entry
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Presence of retained rods or screws or insertion or joint replacement in the joint to be injected
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History of autoimmune diseases including lupus and rheumatoid arthritis
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Prior arthroscopic or open surgery of the index joint within 6 months prior to screening
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Planned arthroscopic or open surgery of the index joint during study period
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Intra-articular injections in the index joint within 3 months prior to screening for corticosteroids or dextrose injections, and within 6 months prior to screening for hyaluronic acid or platelet-rich plasma (PRP) injections
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Use of systemic immunosuppressives, immunomodulators or chemotherapeutic agents within 3 months prior to baseline visit
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Know hypersensitivity to lidocaine, epinephrine or heparin
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History of coagulopathy
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Fever (forehead temperature above 38.0 centigrade) at baseline visit
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Subjects with cutaneous infection at the lipoaspirate or bone marrow aspirate site and/or in the area of the injection at baseline visit
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Subjects with hemoglobin less than 10 g/L
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Subjects with platelet count less than 155x109/L
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Subjects participating in a study of an experimental drug or medical device within 30 days of study entry
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Any medical condition the qualified investigator believes makes the patient unsuitable for the study
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Subjects using warfarin before the screening, with an INR above 3
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Karmy Clinic | Brampton | Ontario | Canada | L6V 1B4 |
Sponsors and Collaborators
- Grigory Karmy
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 01