- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04313894
WHARTON JELLY ORIGINATED MESENCHIAL STEM CELL in GONARTHROSIS (WHAMKO)
THE EFFECTIVENESS of WHARTON JELLY ORIGINATED MESENCHIAL STEM CELL in TREATMENT of KNEE OSTEOARTHRITIS
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.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
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
Enrollment (Anticipated)
Phase
- Phase 2
Contacts and Locations
Study Locations
-
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Kayseri
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Melikgazi, Kayseri, Turkey, 38050
- Recruiting
- Erciyes University Faculty of Medicine
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Contact:
- Ali Eray GUNAY, resisdent
- Phone Number: +905556493401
- Email: alieraygunay@hotmail.com
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Contact:
- İbrahim KARAMAN, docent
- Phone Number: 05327183353
- Email: drikaraman@gmail.com
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Principal Investigator:
- Ahmet Güney, professor
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Principal Investigator:
- Yusuf Özkul, professor
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Principal Investigator:
- Mukerrem B Aycan, Assoc. prof
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Principal Investigator:
- Eren Demirpolat, Assist. prof
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Principal Investigator:
- Ali Eray Günay, Med. Doctor
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Principal Investigator:
- İbrahim Karaman, Assoc prof
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Principal Investigator:
- Zeynep B Gonen, Resident
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Principal Investigator:
- Ebru Ozturk, Resident
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Kellgren-Lawrence Grade II-III OA
- Between 60- 65 years old
- Those with chronic knee pain not undergoing 6 months of conservative treatment
- Body Mass Index: 25-30 kg / m2
- Patients who understand the content of the study
- Patients with written consent form
Exclusion Criteria:
- Patients with Diabetes Mellitus
- Patients with septic table
- Patients with bleeding diathesis
- Patients with HIV and Hepatitis
- Body Mass Index greater than 30 kg / m2 and lower than 25 kg / m2
- Those with congenital axis disorder
- Those with malignancy
- Immunosuppressive
- Lumbar pathological findings
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Stem Cell Therapia Group
A total of 11 patients with Kellgren-Lawrence grade II-III knee OA who were admitted to the outpatient clinic with knee pain and who had received conservative treatment for a period of 6 months and who had not benefited from it will be taken.
Patients will be evaluated 7 (V1-7) during the study period.
Patients who comply with the study criteria will be included in the study.
The clinical, immunological and radiological efficacy of the treatment and clinical improvement will be evaluated in all follow-up patients at the beginning and at the beginning of the treatment.
|
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.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changing of Pain after Wharton Jelly Originated Mesenchial Stem Cell İnjection for one year
Time Frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
|
Pain Evaluation With Visual Analog Scale (min : 0 - max: 10)
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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
Time Frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
|
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).
|
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
Time Frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
|
Short Form 36 (min :0 - max :100)
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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
Time Frame: Before injection and 12 Months after injection
|
Direct Graphy Kellgren-Lawrence classification (0-4) - (0 : Better)
|
Before injection and 12 Months after injection
|
|
Chondral and subchondral Changings after Wharton Jelly Originated Mesenchial Stem Cell İnjection for one year
Time Frame: Before injection and 12 Months after injection
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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.
|
Before injection and 12 Months after injection
|
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Changing of Leptin levels in sinovial fluid after Wharton Jelly Originated Mesenchial Stem Cell İnjection for one year
Time Frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
|
Leptin levels in sinovial fluid (elisa)
|
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
Time Frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
|
Adiponectin levels in sinovial fluid (elisa)
|
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
Time Frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
|
tumor necrosing factor-α levels in sinovial fluid (elisa)
|
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
Time Frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
|
Resistin levels in sinovial fluid (elisa)
|
Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
|
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Changing of interleukin-6 levels in sinovial fluid after Wharton Jelly Originated Mesenchial Stem Cell İnjection for one year
Time Frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
|
interleukin-6 levels in sinovial fluid (elisa)
|
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
Time Frame: Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
|
interleukin-1β levels in sinovial fluid
|
Before injection and 15 Day - 30 Day - 45 Day - 3 months - 6 Months - 12 Months after injection
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: İbrahim Karaman, Asc.Prof, TC Erciyes University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2015/397
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
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