Osteoarthritis (OA) is a progressive disease characterized by degeneration of the joint cartilage, which is involved in the immune system leading to proinflammatory cytokine and metalloproteinase release. Knee osteoarthritis is the most common form. The healing is very slow and the damage is not fully recovered, so the degeneration process continues and no treatment modalities completely remove this process. Various methods are used in the treatment of OA and total joint replacement is performed in the patients with OA recently. Ten patients with Kellgren-Lawrence grade II-III knee OA who had been applied for knee pain and received conservative treatment for 6 months and had no benefit will be taken to study. Patients will be assessed 7 (V1-7) times during the study. Clinical, immunologic and radiological treatment effectiveness and clinical improvement will be evaluated at the beginning of the treatment and in all follow-up patients participating in the study.
Osteoarthritis (OA) is a progressive disease characterized by degeneration of the articular cartilage, caused with the release of proinflammatory cytokines and metalloproteinases. Knee osteoarthritis is the most common form. OA accounts for about 2% of public health problems and leads to a reduction in production, resulting in indirect costs. Regardless of the etiology (age, trauma, overuse, autoimmune arthritis, infection, etc.), the recovery is very slow, the damage is not fully recovered, and the result is secondary fibrosis healing. Therefore, the degeneration process continues and no treatment modality does not completely eliminate this process. Various methods are used in the treatment of OA. The most commonly used of these methods are the physical and educational therapy offered by the American Society of Orthopedic Surgeons (AAOS), symptomatic treatment with acetaminophen and non-steroidal anti-inflammatory drugs, and steroid injection. In patients with end-stage OA who do not benefit from these treatment methods, total joint replacement is performed. Mesenchymal stem cells are multiple potent progenitor cells. In recent years, there have been promising developments in the treatment of patients who cannot be cured by stem cell therapy. Mesenchymal stem cells have been used in clinical and experimental animal studies due to their immunosuppressive effects, limited immunogenetic effects, their ability to be produced in culture and their multilevel structure. At the same time, studies have shown that mesenchymal stem cells have potential to differentiate into osteocytes, chondrocytes, muscle cells and nerve cells. Because of these features, mesenchymal stem cells have been used clinically for OA treatment. In addition, studies have shown that mesenchymal stem cells can be obtained from bone marrow, periosteum, trabecular bone, fat tissue, synovia, muscle tissue, milk tooth, umbilical cord and Wharton gel. Wharton gel is a mucous connective tissue in the umbilical cord and consists of myofibroblast-like stromal cells, collagen fibers, proteoglycans and hyaluronic acid. Because of these properties, it can be used as a source of stem cells. dipocytokines are cytokines secreted from adipose tissue and act as intercellular signal proteins. These cytokines include adipose tissue and cells nutrient uptake, regulation of energy balance, insulin activation, lipid and glucose metabolism, angiogenesis, regulation of blood pressure, coagulation, immunostimulation, pro-inflammatory and anti-inflammatory effects. Stem cell applications are now widely used in different tissues. In the recovery of chondral damage; Since cells have little capacity for regeneration and proliferation, stem cell derived differentiation is needed. In this study, it will be tried to show that chondral damage can be treated with wharton gel-derived stem cells.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
11
In this study, the patient who has no systemic disease from Erciyes University, Obstetrics and Gynecology Department will be taken to the cord transport solution which will be medical waste after delivery. Samples for transport bacteriological tests from the transport solution to the laboratory shall be separated. They will be processed in a number of ways. The cells obtained will be administered intraarticularly at a dose of 1 x 100.000.000.
Erciyes University Faculty of Medicine
Melikgazi, Kayseri, Turkey (Türkiye)
RECRUITINGChanging of Pain after Wharton Jelly Originated Mesenchial Stem Cell İnjection for one year
Pain Evaluation With Visual Analog Scale (min : 0 - max: 10)
Time frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
Changing of functional knee score after Wharton Jelly Originated Mesenchial Stem Cell İnjection for one year
The Western Ontario and McMaster Universities Arthritis Index (WOMAC) measures five items for pain (score range 0-20), two for stiffness (score range 0-8), and 17 for functional limitation (score range 0-68).
Time frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
Changing of life Quality after Wharton Jelly Originated Mesenchial Stem Cell İnjection for one year
Short Form 36 (min :0 - max :100)
Time frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
Radiological Changings according to Kellgren-Lawrence classification systemafter Wharton Jelly Originated Mesenchial Stem Cell İnjection for one year
Direct Graphy Kellgren-Lawrence classification (0-4) - (0 : Better)
Time frame: Before injection and 12 Months after injection
Chondral and subchondral Changings after Wharton Jelly Originated Mesenchial Stem Cell İnjection for one year
Magnetic Resosonans Imaging T2 mapping (msn): If an area have a value above 50/msn that will named as inflamated cartilage. This area's size and mean speed will be evaluated.
Time frame: Before injection and 12 Months after injection
Changing of Leptin levels in sinovial fluid after Wharton Jelly Originated Mesenchial Stem Cell İnjection for one year
Leptin levels in sinovial fluid (elisa)
Time frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
Changing of adiponectin levels in sinovial fluid after Wharton Jelly Originated Mesenchial Stem Cell İnjection for one year
Adiponectin levels in sinovial fluid (elisa)
Time frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
Changing of tumor necrosing factor-α levels in sinovial fluid after Wharton Jelly Originated Mesenchial Stem Cell İnjection for one year
tumor necrosing factor-α levels in sinovial fluid (elisa)
Time frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
Changing of resistin levels in sinovial fluid after Wharton Jelly Originated Mesenchial Stem Cell İnjection for one year
Resistin levels in sinovial fluid (elisa)
Time frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
Changing of interleukin-6 levels in sinovial fluid after Wharton Jelly Originated Mesenchial Stem Cell İnjection for one year
interleukin-6 levels in sinovial fluid (elisa)
Time frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
Changing of interleukin-1β levels in sinovial fluid after Wharton Jelly Originated Mesenchial Stem Cell İnjection for one year
interleukin-1β levels in sinovial fluid
Time frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
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