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The purpose of this study is to determine the safety and efficacy of intraarticular injection of umbilical cord derived Wharton's Jelly for treatment of knee osteoarthritis symptoms.
Osteoarthritis (OA) is the most common joint disorder in the United States (US), affecting approximately 12% (~30 million) of adults aged between 25 and 74 years. By 2030, the number of US adults with arthritis is expected to reach 67 million leading to continuous increase in number of total knee replacement surgeries. While total knee replacement surgeries have shown advantages, avoiding or delaying surgery appears desirable, both from medical and health care system perspective. Lowering the number of total knee replacement surgeries will also lead to a reduced number of costly revision surgeries. Published studies have also demonstrated that the outcomes after total knee replacement surgeries for patients with Grade II or III knee OA (on Kellgren-Lawrence scale) are worse compared to patients with Grade IV OA. Conventional treatment modalities including activity modification, physical therapy, pharmacological agents such as nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, viscosupplementation and narcotics have limitations and potential side effects. Thus, there is a need for alternative intervention for patients with Grade II or III knee OA.
Interest in the use of biologics for regenerative medicine applications has increased over the last decade. To be compliant in the United States (U.S.), biologics that adhere to the U.S. Food and Drug Administration (FDA) regulation of Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/P's) regulated under title 21, part 1271 of the Code of Federal Regulations (CFR) must meet all the conditions under section 361 of Public Health Safety (PHS) Act to be regulated solely under this section. According to this regulation, HCT/P's must meet the criteria of being minimally manipulated, for homologous use only, not to be combination products, to have no systemic effect, and to be non-dependent on the metabolic activity of the living cells. Despite increased use, there is insufficient literature assessing the amount of growth factors (GF), cytokines (CK), hyaluronic acid (HA) and extracellular vesicles (EV) including exosomes present in these products, and more specifically, umbilical cord derived Wharton's Jelly. In addition, there is limited or no literature assessing the safety and efficacy of umbilical cord derived Wharton's Jelly products via a clinical study.
To address the insufficient literature assessing the presence and quantity of GF, CK, HA and EV including exosomes, investigators formulated a novel umbilical cord derived Wharton's Jelly product and evaluated it for the presence of these factors. The results from this study demonstrated that the essential components of regenerative medicine, namely GF, CK, HA and EV, are all present in large quantities in the formulated Wharton's Jelly. This study was an essential preliminary step to better characterize this Wharton's Jelly formulation before performing clinical trials to determine safety and efficacy of this novel formulation for regenerative medicine applications.
The goal of the proposed study is to evaluate the safety and efficacy of intraarticular injection of umbilical cord derived Wharton's Jelly for treatment of knee osteoarthritis symptoms. Investigators also hypothesize that patients receiving intraarticular injection of Wharton's Jelly is safe and will show an improvement in their overall satisfaction, Numeric Pain rating Scale (NPRS), Knee Injury and Osteoarthritis Outcome Score (KOOS) and cartilage formation over a period of 1 year compared to the baseline visit.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Wharton's Jelly | Experimental | Intraarticular injection of Umbilical Cord-derived Wharton's Jelly |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Umbilical Cord-derived Wharton's Jelly | Biological | Intraarticular injection |
|
| Measure | Description | Time Frame |
|---|---|---|
| Treatment-emergent adverse effects as assessed by Comprehensive Metabolic Profile | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by Comprehensive metabolic profile | 1week |
| Treatment-emergent adverse effects as assessed by Comprehensive Metabolic Profile | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by Comprehensive metabolic profile | 6weeks |
| Treatment-emergent adverse effects as assessed by Comprehensive Metabolic Profile | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by Comprehensive metabolic profile | 3months |
| Treatment-emergent adverse effects as assessed by Comprehensive Metabolic Profile | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by Comprehensive metabolic profile | 6months |
| Treatment-emergent adverse effects as assessed by Comprehensive Metabolic Profile | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by Comprehensive metabolic profile | 1year |
| Treatment-emergent adverse effects as assessed by creatinine levels | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by creatinine levels |
| Measure | Description | Time Frame |
|---|---|---|
| Change in patient reported outcome measures, Numeric Pain Rating Scale | To determine change in patient reported outcome measure, Numeric Pain Rating Scale (NPRS). A decrease in score indicates improvement. | Change from baseline to immediately after injection |
| Change in patient reported outcome measures, Numeric Pain Rating Scale |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Saadiq F. El-Amin III, MD, PhD | Contact | 678-257-7078 | dr.saadiqelamin@gmail.com | |
| Ashim Gupta, PhD, MBA | Contact | agupta@biointegrate.com |
| Name | Affiliation | Role |
|---|---|---|
| Saadiq F. El-Amin III, MD, PhD | El-Amin Orthopaedic & Sports Medicine Institute | Principal Investigator |
| Ashim Gupta, PhD, MBA | BioIntegrate | Study Director |
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| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 33602286 | Derived | Gupta A, Maffulli N, Rodriguez HC, Lee CE, Levy HJ, El-Amin SF 3rd. Umbilical cord-derived Wharton's jelly for treatment of knee osteoarthritis: study protocol for a non-randomized, open-label, multi-center trial. J Orthop Surg Res. 2021 Feb 18;16(1):143. doi: 10.1186/s13018-021-02300-0. |
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| ID | Term |
|---|---|
| D020370 | Osteoarthritis, Knee |
| ID | Term |
|---|---|
| D010003 | Osteoarthritis |
| D001168 | Arthritis |
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
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| 1week |
| Treatment-emergent adverse effects as assessed by creatinine levels | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by creatinine levels | 6weeks |
| Treatment-emergent adverse effects as assessed by creatinine levels | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by creatinine levels | 3months |
| Treatment-emergent adverse effects as assessed by creatinine levels | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by creatinine levels | 6months |
| Treatment-emergent adverse effects as assessed by creatinine levels | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by creatinine levels | 1year |
| Treatment-emergent adverse effects as assessed by liver function tests | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by liver function tests | 1week |
| Treatment-emergent adverse effects as assessed by liver function tests | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by liver function tests | 6weeks |
| Treatment-emergent adverse effects as assessed by liver function tests | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by liver function tests | 3months |
| Treatment-emergent adverse effects as assessed by liver function tests | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by liver function tests | 6months |
| Treatment-emergent adverse effects as assessed by liver function tests | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by liver function tests | 1year |
| Treatment-emergent adverse effects as assessed by complete blood count | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by complete blood count | 1week |
| Treatment-emergent adverse effects as assessed by complete blood count | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by complete blood count | 6weeks |
| Treatment-emergent adverse effects as assessed by complete blood count | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by complete blood count | 3months |
| Treatment-emergent adverse effects as assessed by complete blood count | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by complete blood count | 6months |
| Treatment-emergent adverse effects as assessed by complete blood count | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by complete blood count | 1year |
| Treatment-emergent adverse effects as assessed by C-reactive protein | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by C-reactive protein | 1week |
| Treatment-emergent adverse effects as assessed by C-reactive protein | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by C-reactive protein | 6weeks |
| Treatment-emergent adverse effects as assessed by C-reactive protein | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by C-reactive protein | 3months |
| Treatment-emergent adverse effects as assessed by C-reactive protein | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by C-reactive protein | 6months |
| Treatment-emergent adverse effects as assessed by C-reactive protein | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by C-reactive protein | 1year |
| Treatment-emergent adverse effects as assessed by erythrocyte sedimentation rate | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by erythrocyte sedimentation rate | 1week |
| Treatment-emergent adverse effects as assessed by erythrocyte sedimentation rate | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by erythrocyte sedimentation rate | 6weeks |
| Treatment-emergent adverse effects as assessed by erythrocyte sedimentation rate | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by erythrocyte sedimentation rate | 3months |
| Treatment-emergent adverse effects as assessed by erythrocyte sedimentation rate | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by erythrocyte sedimentation rate | 6months |
| Treatment-emergent adverse effects as assessed by erythrocyte sedimentation rate | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by erythrocyte sedimentation rate | 1year |
| Treatment-emergent adverse effects as assessed by T, B and NK cell lymphocyte subsets | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by T, B and NK cell lymphocyte subsets | 1week |
| Treatment-emergent adverse effects as assessed by T, B and NK cell lymphocyte subsets | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by T, B and NK cell lymphocyte subsets | 6weeks |
| Treatment-emergent adverse effects as assessed by T, B and NK cell lymphocyte subsets | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by T, B and NK cell lymphocyte subsets | 3months |
| Treatment-emergent adverse effects as assessed by T, B and NK cell lymphocyte subsets | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by T, B and NK cell lymphocyte subsets | 6months |
| Treatment-emergent adverse effects as assessed by T, B and NK cell lymphocyte subsets | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by T, B and NK cell lymphocyte subsets | 1year |
| Treatment-emergent adverse effects as assessed by serum IgG, IgA, IgM and IgE levels | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by serum IgG, IgA, IgM and IgE levels | 1week |
| Treatment-emergent adverse effects as assessed by serum IgG, IgA, IgM and IgE levels | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by serum IgG, IgA, IgM and IgE levels | 6weeks |
| Treatment-emergent adverse effects as assessed by serum IgG, IgA, IgM and IgE levels | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by serum IgG, IgA, IgM and IgE levels | 3months |
| Treatment-emergent adverse effects as assessed by serum IgG, IgA, IgM and IgE levels | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by serum IgG, IgA, IgM and IgE levels | 6months |
| Treatment-emergent adverse effects as assessed by serum IgG, IgA, IgM and IgE levels | To determine safety i.e. adverse events associated with intraarticular administration of Umbilical cord-derived Wharton's Jelly as assessed by serum IgG, IgA, IgM and IgE levels | 1year |
To determine change in patient reported outcome measure, Numeric Pain Rating Scale (NPRS). A decrease in score indicates improvement. |
| Change from baseline to 24hours after injection |
| Change in patient reported outcome measures, Numeric Pain Rating Scale | To determine change in patient reported outcome measure, Numeric Pain Rating Scale (NPRS). A decrease in score indicates improvement. | Change from baseline to 48hours after injection |
| Change in patient reported outcome measures, Numeric Pain Rating Scale | To determine change in patient reported outcome measure, Numeric Pain Rating Scale (NPRS). A decrease in score indicates improvement. | Change from baseline to 1week after injection |
| Change in patient reported outcome measures, Numeric Pain Rating Scale | To determine change in patient reported outcome measure, Numeric Pain Rating Scale (NPRS). A decrease in score indicates improvement. | Change from baseline to 6weeks after injection |
| Change in patient reported outcome measures, Numeric Pain Rating Scale | To determine change in patient reported outcome measure, Numeric Pain Rating Scale (NPRS). A decrease in score indicates improvement. | Change from baseline to 3months after injection |
| Change in patient reported outcome measures, Numeric Pain Rating Scale | To determine change in patient reported outcome measure, Numeric Pain Rating Scale (NPRS). A decrease in score indicates improvement. | Change from baseline to 6months after injection |
| Change in patient reported outcome measures, Numeric Pain Rating Scale | To determine change in patient reported outcome measure, Numeric Pain Rating Scale (NPRS). A decrease in score indicates improvement. | Change from baseline to 1year after injection |
| Change in patient reported outcome measures, Knee Injury and Osteoarthritis Outcome Score | To determine change in patient reported outcome measure, Knee Injury and Osteoarthritis Outcome Score (KOOS). An increase in score indicates improvement. | Change from baseline to 1week after injection |
| Change in patient reported outcome measures, Knee Injury and Osteoarthritis Outcome Score | To determine change in patient reported outcome measure, Knee Injury and Osteoarthritis Outcome Score (KOOS). An increase in score indicates improvement. | Change from baseline to 6weeks after injection |
| Change in patient reported outcome measures, Knee Injury and Osteoarthritis Outcome Score | To determine change in patient reported outcome measure, Knee Injury and Osteoarthritis Outcome Score (KOOS). An increase in score indicates improvement. | Change from baseline to 3months after injection |
| Change in patient reported outcome measures, Knee Injury and Osteoarthritis Outcome Score | To determine change in patient reported outcome measure, Knee Injury and Osteoarthritis Outcome Score (KOOS). An increase in score indicates improvement. | Change from baseline to 6months after injection |
| Change in patient reported outcome measures, Knee Injury and Osteoarthritis Outcome Score | To determine change in patient reported outcome measure, Knee Injury and Osteoarthritis Outcome Score (KOOS). An increase in score indicates improvement. | Change from baseline to 1year after injection |
| Cartilage Formation | To assess cartilage formation via MOCART (Magnetic Resonance Observation of Cartilage Repair Tissue). An increase in score indicates improvement. | Change from baseline to 1year after injection |
| Patient Satisfaction via 36-item short form survey (SF36) | To determine patient satisfaction via 36-item short form survey (SF36) | Change from baseline to 3Months after injection |
| Patient Satisfaction via 36-item short form survey (SF36) | To determine patient satisfaction via 36-item short form survey (SF36) | Change from baseline to 6Months after injection |
| Patient Satisfaction via 36-item short form survey (SF36) | To determine patient satisfaction via 36-item short form survey (SF36) | Change from baseline to 1year after injection |
| Patient Satisfaction via 7-point Likert Scale | To determine patient satisfaction via 7-point Likert Scale. An increase in score indicates improvement. | 1week after injection |
| Patient Satisfaction via 7-point Likert Scale | To determine patient satisfaction via 7-point Likert Scale. An increase in score indicates improvement. | 6weeks after injection |
| Patient Satisfaction via 7-point Likert Scale | To determine patient satisfaction via 7-point Likert Scale. An increase in score indicates improvement. | 3months after injection |
| Patient Satisfaction via 7-point Likert Scale | To determine patient satisfaction via 7-point Likert Scale. An increase in score indicates improvement. | 6months after injection |
| Patient Satisfaction via 7-point Likert Scale | To determine patient satisfaction via 7-point Likert Scale. An increase in score indicates improvement. | 1year after injection |
| Patient Satisfaction via Single Assessment Numeric Evaluation (SANE) | To determine patient satisfaction via Single Assessment Numeric Evaluation (SANE). An increase in score indicates improvement. | Change from baseline to 1week after injection |
| Patient Satisfaction via Single Assessment Numeric Evaluation (SANE) | To determine patient satisfaction via Single Assessment Numeric Evaluation (SANE). An increase in score indicates improvement. | Change from baseline to 6weeks after injection |
| Patient Satisfaction via Single Assessment Numeric Evaluation (SANE) | To determine patient satisfaction via Single Assessment Numeric Evaluation (SANE). An increase in score indicates improvement. | Change from baseline to 3months after injection |
| Patient Satisfaction via Single Assessment Numeric Evaluation (SANE) | To determine patient satisfaction via Single Assessment Numeric Evaluation (SANE). An increase in score indicates improvement. | Change from baseline to 6months after injection |
| Patient Satisfaction via Single Assessment Numeric Evaluation (SANE) | To determine patient satisfaction via Single Assessment Numeric Evaluation (SANE). An increase in score indicates improvement. | Change from baseline to 1year after injection |
| D012216 |
| Rheumatic Diseases |