WHARTON JELLY ORIGINATED MESENCHIAL STEM CELL in GONARTHROSIS (WHAMKO)

March 17, 2020 updated by: İbrahim Karaman, TC Erciyes University

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

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

Interventional

Enrollment (Anticipated)

11

Phase

  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Kayseri
      • Melikgazi, Kayseri, Turkey, 38050
        • Recruiting
        • Erciyes University Faculty of Medicine
        • Contact:
        • Contact:
        • Principal Investigator:
          • Ahmet Güney, professor
        • Principal Investigator:
          • Yusuf Özkul, professor
        • Principal Investigator:
          • Mukerrem B Aycan, Assoc. prof
        • Principal Investigator:
          • Eren Demirpolat, Assist. prof
        • Principal Investigator:
          • Ali Eray Günay, Med. Doctor
        • Principal Investigator:
          • İbrahim Karaman, Assoc prof
        • Principal Investigator:
          • Zeynep B Gonen, Resident
        • Principal Investigator:
          • Ebru Ozturk, Resident

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

56 years to 61 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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.

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)
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)
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
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
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
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

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: İbrahim Karaman, Asc.Prof, TC Erciyes University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2019

Primary Completion (Actual)

December 31, 2019

Study Completion (Anticipated)

December 31, 2020

Study Registration Dates

First Submitted

February 9, 2019

First Submitted That Met QC Criteria

March 17, 2020

First Posted (Actual)

March 18, 2020

Study Record Updates

Last Update Posted (Actual)

March 18, 2020

Last Update Submitted That Met QC Criteria

March 17, 2020

Last Verified

March 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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