Use of Adipose Tissue Derived Mesenchymal Stem Cells for Knee Osteoarthrosis

Phase 1

• Conditions: Knee Osteoarthrosis
• Interventions: Biological: Adipose tissue derived mesenchymal stem cell

• Registration Number: NCT02966951
• Lead Sponsor: Hanan Jafar

Brief Summary

Adipose tissue derived Mesenchymal Stem cells (ATMSC) will be injected in patients diagnosed with Knee osteoarthrosis

Detailed Description

Ten patients from both genders diagnosed with Knee osteoarthrosis, will be enrolled according to specific inclusion and exclusion criteria. These patients will be injected with Adipose Tissue derived Mesenchymal Stem Cells. Then, they are followed by clinical assessment, laboratory investigations as well as magnetic resonance imaging (MRI) of the injected knee.

Study Timeline

• Study First Submitted: 2016-11-15
• Study First Submitted QC: 2016-11-15
• Study First Posted: 2016-11-17
• Study Start: 2017-01-17
• Status Verified: 2021-04
• Last Update Submitted: 2021-04-27
• Last Update Posted: 2021-04-28
• Primary Completion: 2021-09
• Study Completion: 2021-12

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

Severe KOA stage III or IV by Laurance & Kellgren staging as judged by Posterioranterior (PA) Xray of the knee joint.

Willing to participate by signing the informed consent

Exclusion Criteria

• Sublaxation beyond 20 degrees of the bones of the knee joint
• Oral anticoagulants or heparin therapy
• Heart failure or arrhythmia
• Body Mass Index > 35
• Uncontrolled Diabetes Mellitus.
• Evidence of Infectious Diseases.
• Active infection
• Malignancy
• Pregnancy
• Anemia less than 11g/dl or thrombocytopenia less than 100,000 or leucopenia less than 3000.
• Unreliable patients
• Non-resident in Jordan

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
adipose tissue mesenchymal stem cell	Adipose tissue derived mesenchymal stem cell	Intra-articular adipose tissue derived mesenchymal stem cell injection will be given for each patient in 2 doses, 50 million of ATMSC in each dose

Primary Outcome Measures

Name	Time	Method
Evaluation of the safety and tolerability of the intra articular injection	Time Frame: 6 months	patients will be monitored for any adverse events resulting from the intraarticular injection of ATMSC

Secondary Outcome Measures

Name	Time	Method
Assessment of the efficacy of intra-articular injection of ATMSC	12 months	The efficacy of the intra-articular injection of ATMSC will be assessed by Magnetic Resonance Imaging (MRI).

Trial Locations

Locations (1)

Cell Therapy Center; 🇯🇴 Amman, Jordan