Osteoarthritis Clinical Trial
Official title:
Treatment of Osteoarthritis With the Stromal Vascular Fraction of Abdominal Adipose Tissue - a Pilot Study
To investigate the feasibility and short term safety issues of treatment of knee
osteoarthritis with intra-articular injection with the stromal vascular fraction of abdominal
adipose tissue (SVF) harvested and prepared using the Lipogems System.
Hereby we wish to pave the road for a high quality randomized controlled trial investigating
effectiveness of treatment of knee osteoarthritis with SVF looking at patient reported
outcome, function, homeostasis of the joint and cartilage regeneration.
Background Osteoarthritis (OA) of the knee is a destructive joint disease, causing
degeneration of cartilage, damage to the underlying bone and morphological changes to the
joint1. It is a major public health concern due to the increased life expectancy of the
ageing population2,3. No approved medical treatment that reverses the morphological changes
currently exists. Conventional treatment includes physiotherapy, pain killers, braces and in
end-stage OA surgical knee replacement4.
Treatment of Osteoarthritis with Paqe 3 Version 2 the Stromal Vascular Fraction of Adipose
tissue 02-11-2015 During the past decade researchers have started to explore the regenerative
potential of mesenchymal stem cells (MSC) in OA5. MSCs are multipotent progenitor cells able
to give rise to osteocytes, adipocytes, chondrocytes, myoblasts and tenocytes6. MSCs were
first used to treat Chondral defects in 19987 and to treat OA in 20028. Since, a number of
case reports and prospective series have been published showing significant short term and
long term effect on pain and cartilage thickness5. Recently a prospective case-series of 1128
patients involving 1856 joints were treated with the stromal vascular fraction of abdominal
Adipose tissue (SVF) which is a rich source of mesenchymal stem cells. 86% of the treated
patients showed an improvement of at least 50% in modified Knee/Hip Osteoarthritis Outcome
Score (KOOS/HOOS) at 3 months and 129. Only 0.9% of patients were non-responders showing no
improvement after treatment. No serious adverse effects like infection or tumor formation
were observed9, which is in accordance with previous studies10. Non-manipulated or minimally
manipulated cell therapies have been used within a wide range of medical conditions
including: stroke, myocardial infarction, Crohn's disease, rheumatoid arthritis and breast
augmentation. More than 17,000 scientific articles have been published reporting treatment of
more than 320,000 patients11. No severe safety issues have been raised12.
Mesenchymal stem cells can be derived from bone marrow or adipose tissue5. Most research has
been performed on bone marrow-derived stem cells but the past years a series of studies have
been published showing promising effect of Adipose-derived mesenchymal stem cells (AMSCs). By
using AMSC a large amount of cells can be harvested from a small volume of tissue thereby
avoiding the costly and time consuming process of expanding the cells in culture5,9.
Abdominal adipose tissue has been shown to have a 1000 times higher concentration of AMSC
than other investigated adipose tissue9. This opens for the possibility of a one-step
procedure where cells are harvested and injected during one visit in the outpatient clinic.
The optimal dose of AMSC is unknown but the effect seems to be dose-dependent with doses
around 1.0 x 108 AMSCs per injection being desirable5,9. The stromal vascular fraction of
abdominal Adipose tissue is a rich source of adipose derived mesenchymal stem cells.
In 2014 the Lipogems system has been launched as a commercial of-the-shelf product:
http://lipogems.eu/. The Lipogems system is an enzyme-free technology developed to process
lipoaspirates in a closed system, resulting in a non-expanded adipose tissue product that
contains SVF13. Before using this product in larger scale a controlled study of its
feasibility and safety is needed.
Study Objective To investigate the feasibility and short term safety issues of treatment of
knee osteoarthritis with intra-articular injection with the stromal vascular fraction of
abdominal adipose tissue (SVF) harvested and prepared using the Lipogems System.
Hereby we wish to pave the road for a high quality randomized controlled trial investigating
effectiveness of treatment of knee osteoarthritis with SVF looking at patient reported
outcome, function, homeostasis of the joint and cartilage regeneration.
6 Treatment Patients participating in the study are treated according to the Danish National
Clinical Guidelines for people with osteoarthritis16. They receive three months of
physiotherapy, are guided concerning the optimal pharmaceutical treatment with painkillers
and people with BMI above 28 are offered a consultation with a dietitian.
6.1 Description of the active treatment The active treatment is an intra-articular injection
with the stromal vascular fraction (SVF) harvested from the patient's own abdominal
subcutaneous fatty tissue. SVF is harvested using the Lipogems system.
6.1.1 Harvest of SVF Harvest of SVF is done under sterile conditions in the outpatient
clinic. The patient is positioned supine on an examination bench. The area from which the
tissue will be harvested is marked on the skin with a surgical marker. The area is app. 8cm
(cranio-caudal) x 20cm (lateral) and situated just below the umbilicus. Local anesthesia is
applied to the whole area with a suspension of Carbocain 1%, 200ml isotonic saline,
adrenaline and 10mmol Bicarbonate. Surgical cleaning is performed twice and a sterile draping
is applied. Through a stab incision the harvesting needle is introduced to the subcutaneous
fat and suction is applied. 20ml to 40ml of subcutaneous adipose tissue is harvested. At the
end of the procedure the skin is closed with a plaster.
6.1.2 Preparation of SVF for implantation The syringes with subcutaneous aspirate are
prepared using the Lipogems system. The Lipogems system is an enzyme-free technology
developed to process variable amounts of lipoaspirates in a closed system, resulting in a
nonexpanded adipose tissue product that contains SVF. The technology works through a mild
mechanical tissue cluster size reduction. Thereby avoiding the use of any enzyme and
additional processing (i.e., centrifugation and subfractional harvesting).13 6.1.3
Implantation of SVF Implantation of the SVF is done under sterile conditions in the
outpatient clinic. The patient is positioned supine on an examination bench with the affected
knee stretched. The superior pole of the patella is palpated and the femoral condyle is
marked with a surgical marker. The suprapattelar recess is located by ultrasound, local
anesthesia is applied to the injection site and surgical cleaning is performed twice.
Injection of the SVF in to the suprapattelar recess is done using a 21 gauge syringe under
direct visualization by ultrasound. At the end of the procedure the skin is closed with a
plaster.
6.1.4 Control of dose of injected SVF Control of the dose of AMSC in the injected SVF is
performed after injection. As a consequence of the logistical favorable setup where harvest
and implantation is performed in a one-step procedure it is not possible to count the AMSC
before injection. Instead one mL of the solution is sent for cell count in the pathological
department.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04657926 -
A Trial of APPA in the Treatment of Knee Osteoarthritis
|
Phase 2 | |
Completed |
NCT02536833 -
A Study Evaluating the Safety, Tolerability, and Efficacy of SM04690 Injected in the Target Knee Joint of Moderately to Severely Symptomatic Osteoarthritis Subjects
|
Phase 2 | |
Completed |
NCT03014037 -
Comparing Mesenchymal Stem Cell Counts in Unilateral vs. Bilateral Posterior Superior Iliac Spine Bone Marrow Aspiration
|
N/A | |
Recruiting |
NCT05937542 -
A Qualitative Investigation of CLEAT Participants
|
||
Completed |
NCT03644615 -
A Mindfulness Program (MBSR) in the Management of Symptomatic Hip and Knee Osteoarthritis
|
N/A | |
Recruiting |
NCT06061367 -
Muscles Strength and Gait Parameteres After TKA
|
||
Withdrawn |
NCT04976972 -
A Comparison of Patients Receiving a Total Knee Replacement With Robotic Assistance or With Conventional Instrumentation
|
N/A | |
Completed |
NCT05496205 -
A SAD Study to Evaluate the Safety, Tolerability and PK/PD of iN1011-N17 in Healthy Volunteers
|
Phase 1 | |
Completed |
NCT03850665 -
Comparison of Functional Outcome in Patients After Hip Arthroplasty Depending on Surgical Approach
|
N/A | |
Completed |
NCT02826902 -
Effect of Anesthesia on Quality of Recovery in Patients Undergoing Correctional Tibial Osteotomy - A Randomized Controlled Trial
|
N/A | |
Completed |
NCT04402502 -
Dynamic 4DCT to Examine Wrist Carpal Mechanics
|
N/A | |
Completed |
NCT02923700 -
Leukocyte-rich PRP vs Leukocyte-poor PRP for the Treatment of Knee Cartilage Degeneration: a Randomized Controlled Trial
|
Phase 4 | |
Completed |
NCT04564053 -
Study of Safety, Tolerability and Pharmacokinetics of LNA043 in Japanese Osteoarthritis Participants
|
Phase 1 | |
Completed |
NCT05070871 -
A Clinical Trial Investigating the Effect of Salmon Bone Meal on Osteoarthritis Among Men and Women
|
N/A | |
Not yet recruiting |
NCT05036174 -
Diphenhydramine Ointment for Knee Osteoarthritis
|
N/A | |
Recruiting |
NCT02912429 -
Onlay vs. Inlay Patellofemoral Arthroplasty
|
N/A | |
Recruiting |
NCT02666443 -
Low Dose Dexamethasone in Supraclavicular Blocks
|
N/A | |
Active, not recruiting |
NCT02723929 -
Effects of tDCS and tUS on Pain Perception in OA of the Knee
|
||
Withdrawn |
NCT02921594 -
Kinematic Comparison of Vanguard XP and Vanguard CR Total Knee Arthroplasties
|
N/A | |
Terminated |
NCT02820766 -
Journey II BCS CMS Total Knee System Compared to Other PS Total Knee Systems in PT Setting
|
N/A |