Knee osteoarthritis (OA) is a leading cause of disability. The objectives of treatment are to reduce pain, improve function, and slow down further breakdown of the knee. Recently, research on nonsurgical treatment options for knee OA has increased significantly. One potential treatment of interest is the use of stem cell injections. Stem cells are one's own cells that have the ability to divide into other types of cells, and may cause regrowth of cartilage when injected into the knee. There have been few, but promising, studies that show improvements in pain and function with stem cell injections in those with knee OA. Therefore, more research is needed to identify patients who might benefit from this injection. This pilot study will look at changes in pain and function for 20 patients at 1, 3, 6, and 12 months after a stem cell injection into the knee. Patients will also undergo magnetic resonance imaging at 6 months and 12 months following the injection.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
13
Bone marrow will be aspirated from the iliac crest and injected into the knee.
Bone marrow will be aspirated from the iliac crest.
Hospital for Special Surgery
New York, New York, United States
Knee Injury and Osteoarthritis Outcome Score (KOOS) Jr.
The KOOS Jr. measures patient-reported pain and function. The score ranges from 0-100, with 0 representing total knee disability and 100 representing perfect knee health.
Time frame: 1 month after date of injection
KOOS Jr.
The KOOS Jr. measures patient-reported pain and function. The score ranges from 0-100, with 0 representing total knee disability and 100 representing perfect knee health.
Time frame: 3 months after date of injection
KOOS Jr.
The KOOS Jr. measures patient-reported pain and function. The score ranges from 0-100, with 0 representing total knee disability and 100 representing perfect knee health.
Time frame: 6 months after date of injection
KOOS Jr.
The KOOS Jr. measures patient-reported pain and function. The score ranges from 0-100, with 0 representing total knee disability and 100 representing perfect knee health.
Time frame: 12 months after date of injection
Pain
Pain will be assessed using the numerical rating scale (NRS), which is on a scale of 0-10. 10 represents worst pain, and 0 represents no pain.
Time frame: 1 month, 3 months, 6 months, and 12 months after date of injection
Degree of cartilage change
Cartilage change will be assessed via magnetic resonance imaging.
Time frame: 6 months (first 5 patients only) and 12 months after date of injection
Presence of side effects
The presence of side effects, including increased pain, bleeding, infection, and motor-sensory deficits, will be documented.
Time frame: 1 month, 3 months, 6 months, and 12 months after date of injection
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