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Cellular & Biocellular Regenerative Therapy in Musculoskeletal Pain, Dysfunction,Degenerative or Inflammatory Disease (BRT)

Primary Purpose

Osteoarthritis, Rheumatoid Nodule, Degenerative Joint Disease

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Normal Saline
Tissue Stromal Vascular Fraction
Platelet Rich Plasma
Cellular Stromal Vascular Fraction
Sponsored by
Robert W Alexander, MD
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis focused on measuring Arthritis, Degenerative, Tendinosis, Jont disease, Low back pain

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with documented inflammatory, autoimmune (rheumatoid arthritis (RA), degeneration of musculoskeletal system
  • No systemic disorders which, in the opinion of the principal investigators or provider, would disqualify from being safely able to undergo needed procedures
  • Able to provide informed consent
  • Patient having adequate donor adipose (fat) tissue
  • Patient mature enough to tolerate the needed procedures

Exclusion Criteria:

  • Systemic or psychological impairment which would preclude patient tolerance and understanding of procedures and follow up
  • Patients with known active cancer and chemotherapy or radiation therapy
  • Patients with ongoing active infections
  • High dose steroid users or use of injections of corticoid steroids within a six month timeframe
  • Opiate addition or in treatment program for withdrawal
  • History of severe traumatic brain injuries
  • If, in the opinion of providers, the patient will not be able to fully cooperate or complete the study and its follow up

Sites / Locations

  • Regeneris MedicalRecruiting
  • Regeneris MedicalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

tSVF + PRP Arm1

tSVF + PRP + cSVF Enrichment Arm 2

Normal Saline IV + cSVF Arm 3

Arm Description

Stromal Vascular Fraction tSVF + Platelet Rich Plasma (PRP) concentrate

tissue Stromal Vascular Fraction (tSVF) + Platelet-Rich Plasma (PRP) concentration + (cSVF)

Cellular Stromal Vascular Fraction (cSVF); Normal Saline IV introduction

Outcomes

Primary Outcome Measures

Participants with complications
Adverse and Severe Adverse Events Reports

Secondary Outcome Measures

Change from baseline quality of life level (QoL Questionnaire)
QoL Questionnaire
Change from baseline visual analog pain score
Changes of Visual Analog Pain Score (VAS) 1-10
Change from baseline of limitation of activities (Functional analysis of range of motion)
Functional analysis of range of motion compared from baseline
Change from baseline of imaging if required for study entry
imaging

Full Information

First Posted
March 6, 2017
Last Updated
January 13, 2020
Sponsor
Robert W Alexander, MD
Collaborators
Regeneris Medical, Global Alliance for Regenerative Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT03090672
Brief Title
Cellular & Biocellular Regenerative Therapy in Musculoskeletal Pain, Dysfunction,Degenerative or Inflammatory Disease
Acronym
BRT
Official Title
Use of Cellular and Biocellular Therapy in Musculoskeletal Pain, Dysfunction, Degenerative or Inflammatory Disease
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
March 11, 2017 (Actual)
Primary Completion Date
August 31, 2021 (Anticipated)
Study Completion Date
December 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Robert W Alexander, MD
Collaborators
Regeneris Medical, Global Alliance for Regenerative Medicine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Musculoskeletal disorders and degeneration represent injuries or pain in the body's joint ligaments, tendons, muscles, nerves, and skeletal elements that support extremities, spine and related tissues. Direct injuries and aging contribute to breakdown and inflammation of these tissues, leading to debilitation and loss of function in these areas. This has major impact on quality of life, occupational/recreation limitations, and psychosocial implications. Many therapies have been employed including medications, physical therapy, occupational therapy, and a variety of surgical interventions each of which have distinct limitations, often covering the issues versus providing actual healing and return to function. Many reports are now available utilizing self-healing options which include use of stem/stromal cellular therapy or biocellular treatments (either from adipose or marrow) using targeted placement of cells, matrix and platelet concentrates. Termed cellular or Biocellular therapy (typically optimized using ultrasound guidance). It is proposed that use of cellular isolates or cell-stroma derived from the largest deposit of these cells (adipose greater than marrow), may use in conjunction with targeted placement or as a stand alone methodology intravascular use. This study is designed as a interventional means to examine the safety and efficacy of the use of cellular and tissue stromal vascular fraction in musculoskeletal pain, dysfunction degeneration or inflammatory disorders.
Detailed Description
Musculoskeletal disorders and degeneration represent injuries or pain in the body's joint ligaments, tendons, muscles, nerves, and skeletal elements that support extremities, spine and related tissues. Direct injuries and aging contribute to breakdown and inflammation of these tissues, leading to debilitation and loss of function in these areas. This has major impact on quality of life, occupational/recreation limitations, and psychosocial implications. Many therapies have been employed including medications, physical therapy, occupational therapy, and a variety of surgical interventions each of which have distinct limitations, often covering the issues versus providing actual healing and return to function. Many reports are now available utilizing self-healing options which include use of stem/stromal cells (either from adipose or marrow) using targeted placement of cells, matrix and platelet concentrates. This is termed Biocellular therapy, and typically is optimized by use of ultrasound guidance. It is proposed that use of cellular isolates derived from the largest deposit of these cells (adipose greater than marrow), may use in conjunction with targeted placement or as a stand alone methodology of parenteral use. This study is designed as a interventional means to examine the safety and efficacy of the use of cellular stromal vascular fraction (cSVF) in musculoskeletal pain, dysfunction degeneration or inflammatory disorders. The important cellular components represent, not the adipocyte, but the heterogeneous cell group associated with the peri-vasculature. The group does include certain cells referred to as "stem" or "stromal" cells, and are considered key elements of cellular and biocellular treatments. The carrier microvascular tissue, adipose, has been shown to not participate in wound healing or cellular replacement per se. It is well established that those perivascular (adventitial) cell types are found in essentially all tissues of the body, but in highest numbers in the easily accessed depots with the subdermal fat. It is proposed that areas of these groups are responded to as a result of "signaling" to permit a chemotactic request for needed growth factors and cytokines which effectively contribute to the healing capability at failing or damaged sites. This Trial will investigate the safety/efficacy of either combining specific targeting (ultrasound) with and/or without systemic parenteral route introduction. This study includes closed syringe, disposable microcannula harvesting of subdermal fat tissues for obtaining the native perivascular stromal elements (extracellular matrix (ECM) and periadventitial cells shown to be multipotent (in potentials), incubation, digestion and isolation of cSVF. This isolated and concentration of stem/stromal cellular pellet (without actual extracellular matrix or stromal scaffolding elements) is then suspended in 500 cc sterile Normal Saline (NS) and deployed via peripheral intravenous route. Evaluations of safety issues are measured at intervals (both severe and non-severe categories) and by ultrasound and imaging studies. Biocellular treatments are defined as use of tissue stromal vascular fraction (tSVF) obtained within adipose tissue complex (ATC), combined with high density platelet rich plasma (HD PRP) concentrated from standard blood draw. Concentration in FDA approved platelet concentrate devices to achieve levels of >4 times patient's own measured baseline levels. Such concentrates have been shown to provide important growth factors and cytokines (signal proteins) naturally involved in wound healing and repair functions. A form of Cell-Enriched Biocellular Therapy (CEBT) is available as a component of this study, in which the tSVF + HD PRP can be enhanced in cellular numbers via the process of isolating and concentrating cSVF discussed above. Many small case series and case reports have been published in the peer reviewed medical literature which suggest that these interventions are both safe and effective at relieving musculoskeletal disorders included in the study. This study in intended to provide evidence of a non-drug safety and efficacy using both of these interventions. Evaluation and tracking of adverse events or severe adverse events (SAE) will be tracked according to intervals described. Examination of the optimal numbers of cells, viability of such cells, and evaluation of the efficacy will be statistically studied reported relative outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Rheumatoid Nodule, Degenerative Joint Disease, Tendinopathy, Tendinosis, Back Pain
Keywords
Arthritis, Degenerative, Tendinosis, Jont disease, Low back pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
tSVF + PRP Arm1
Arm Type
Experimental
Arm Description
Stromal Vascular Fraction tSVF + Platelet Rich Plasma (PRP) concentrate
Arm Title
tSVF + PRP + cSVF Enrichment Arm 2
Arm Type
Experimental
Arm Description
tissue Stromal Vascular Fraction (tSVF) + Platelet-Rich Plasma (PRP) concentration + (cSVF)
Arm Title
Normal Saline IV + cSVF Arm 3
Arm Type
Experimental
Arm Description
Cellular Stromal Vascular Fraction (cSVF); Normal Saline IV introduction
Intervention Type
Drug
Intervention Name(s)
Normal Saline
Intervention Description
Normal Saline IV delivery
Intervention Type
Procedure
Intervention Name(s)
Tissue Stromal Vascular Fraction
Intervention Description
tSVF
Intervention Type
Biological
Intervention Name(s)
Platelet Rich Plasma
Intervention Description
PRP
Intervention Type
Procedure
Intervention Name(s)
Cellular Stromal Vascular Fraction
Intervention Description
cSVF
Primary Outcome Measure Information:
Title
Participants with complications
Description
Adverse and Severe Adverse Events Reports
Time Frame
1 month
Secondary Outcome Measure Information:
Title
Change from baseline quality of life level (QoL Questionnaire)
Description
QoL Questionnaire
Time Frame
6 months, 12 months
Title
Change from baseline visual analog pain score
Description
Changes of Visual Analog Pain Score (VAS) 1-10
Time Frame
6 months, 1 year, 2 year
Title
Change from baseline of limitation of activities (Functional analysis of range of motion)
Description
Functional analysis of range of motion compared from baseline
Time Frame
baseline, 6 months, 1 year
Title
Change from baseline of imaging if required for study entry
Description
imaging
Time Frame
baseline, 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with documented inflammatory, autoimmune (rheumatoid arthritis (RA), degeneration of musculoskeletal system No systemic disorders which, in the opinion of the principal investigators or provider, would disqualify from being safely able to undergo needed procedures Able to provide informed consent Patient having adequate donor adipose (fat) tissue Patient mature enough to tolerate the needed procedures Exclusion Criteria: Systemic or psychological impairment which would preclude patient tolerance and understanding of procedures and follow up Patients with known active cancer and chemotherapy or radiation therapy Patients with ongoing active infections High dose steroid users or use of injections of corticoid steroids within a six month timeframe Opiate addition or in treatment program for withdrawal History of severe traumatic brain injuries If, in the opinion of providers, the patient will not be able to fully cooperate or complete the study and its follow up
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ryan JP Welter, MD, PhD
Phone
508.345.5492
Email
r.welter@regenerismedical.com
First Name & Middle Initial & Last Name or Official Title & Degree
Gabrielle Lewis
Phone
508.316.4268
Email
g.lewis@regenerismedical.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert W Alexander, MD
Organizational Affiliation
GARM USA
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Glenn C Terry, MD
Organizational Affiliation
Global Alliance for Regenerative Medicine (GARM)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ryan JP Welter, MD, PhD
Organizational Affiliation
Regeneris Medical
Official's Role
Principal Investigator
Facility Information:
Facility Name
Regeneris Medical
City
North Attleboro
State/Province
Massachusetts
ZIP/Postal Code
02760
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gabrielle Lewis
Phone
508-316-4268
Email
g.lewis@regenerismedical.com
First Name & Middle Initial & Last Name & Degree
Gabielle lEWIS
Phone
508/316.4268
Email
g.lewis@regenerismedical.com
Facility Name
Regeneris Medical
City
North Attleboro
State/Province
Massachusetts
ZIP/Postal Code
02760
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ryan JP Welter, MD
Phone
508-345-5492
Email
r.welter@regenerismedical.com
First Name & Middle Initial & Last Name & Degree
Gabrielle Lewis
Phone
508.316.4268
Email
g.lewis@regenerismedical.com
First Name & Middle Initial & Last Name & Degree
Glenn C Terry, MD
First Name & Middle Initial & Last Name & Degree
Robert W Alexander, MD
First Name & Middle Initial & Last Name & Degree
Ryan JP Welter, MD,PhD

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Comparative analysis of safety and efficacy between use of ultrasound guided tissue stromal vascular fraction (AD-tSVF) plus high density platelet rich plasma (HD-PRP) with use of intravascular deployment of adipose-derived cellular stromal vascular fraction (AD-cSVF)
Citations:
PubMed Identifier
15676628
Citation
Kuorinka I, Jonsson B, Kilbom A, Vinterberg H, Biering-Sorensen F, Andersson G, Jorgensen K. Standardised Nordic questionnaires for the analysis of musculoskeletal symptoms. Appl Ergon. 1987 Sep;18(3):233-7. doi: 10.1016/0003-6870(87)90010-x.
Results Reference
background
PubMed Identifier
23516797
Citation
Gallagher S, Heberger JR. Examining the interaction of force and repetition on musculoskeletal disorder risk: a systematic literature review. Hum Factors. 2013 Feb;55(1):108-24. doi: 10.1177/0018720812449648.
Results Reference
background
Citation
Alexander, Robert W., Understanding Mechanical Emulsification (NanoFat) Versus Enzymatic Isolation fo Tissue Stromal Vascular Fraction (tSVF) From Adipose Tissue: Potential Uses in Biocellular Regenerative Medicine. J of Prolo. 2016; 8: 3947-960.
Results Reference
background
PubMed Identifier
27788905
Citation
Alexander RW. Biocellular Regenerative Medicine: Use of Adipose-Derived Stem/Stromal Cells and It's Native Bioactive Matrix. Phys Med Rehabil Clin N Am. 2016 Nov;27(4):871-891. doi: 10.1016/j.pmr.2016.06.005.
Results Reference
background
Citation
Alderman, D, Alexander, R.W.,: Advances In Regenerative Medicine: High Density Platelet-Rich Plasma and Stem Cell Prolotherapy. J Pract Pain Management, 2011; Vol Oct: 49-90
Results Reference
background
Citation
Alexander, Robert W., Understanding Adipose-Derived Stromal Vascular Fraction (SVF) Cell Biology On The Basis of Perivascular Cell Components In Aesthetic and Regenerative Medicine. J. Prolo; 2012; 4: e13777
Results Reference
background
PubMed Identifier
23630430
Citation
Alexander RW, Harrell DB. Autologous fat grafting: use of closed syringe microcannula system for enhanced autologous structural grafting. Clin Cosmet Investig Dermatol. 2013 Apr 8;6:91-102. doi: 10.2147/CCID.S40575. Print 2013.
Results Reference
background
PubMed Identifier
24387819
Citation
Nelson AE, Allen KD, Golightly YM, Goode AP, Jordan JM. A systematic review of recommendations and guidelines for the management of osteoarthritis: The chronic osteoarthritis management initiative of the U.S. bone and joint initiative. Semin Arthritis Rheum. 2014 Jun;43(6):701-12. doi: 10.1016/j.semarthrit.2013.11.012. Epub 2013 Dec 4.
Results Reference
background
PubMed Identifier
24792949
Citation
Katz JN, Brownlee SA, Jones MH. The role of arthroscopy in the management of knee osteoarthritis. Best Pract Res Clin Rheumatol. 2014 Feb;28(1):143-56. doi: 10.1016/j.berh.2014.01.008.
Results Reference
background
PubMed Identifier
26080045
Citation
Thorlund JB, Juhl CB, Roos EM, Lohmander LS. Arthroscopic surgery for degenerative knee: systematic review and meta-analysis of benefits and harms. BMJ. 2015 Jun 16;350:h2747. doi: 10.1136/bmj.h2747.
Results Reference
background
PubMed Identifier
22925619
Citation
Burdett N, McNeil JD. Difficulties with assessing the benefit of glucosamine sulphate as a treatment for osteoarthritis. Int J Evid Based Healthc. 2012 Sep;10(3):222-6. doi: 10.1111/j.1744-1609.2012.00279.x.
Results Reference
background
Citation
Oliver, K., Alexander, RW. Combination of Autologous Adipose-Derived Tissue Stromal Vascular Fraction Plus High Density Platelet-Rich Plasma or Bone Marrow Concentrates in Achilles Tendon Tears. J. Prolo; 2013; 5: e895-912.
Results Reference
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Cellular & Biocellular Regenerative Therapy in Musculoskeletal Pain, Dysfunction,Degenerative or Inflammatory Disease

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