MedPath

Outcomes Data of Adipose Stem Cells to Treat Osteoarthritis

Conditions
Osteoarthritis
Registration Number
NCT02241408
Lead Sponsor
StemGenex
Brief Summary

The purpose of this study is to determine the impact that treatment with a cellular concentrate derived from an individual's own fat, known as the stromal vascular fraction (SVF), has on joint pain and functionality in people with Osteoarthritis (OA). SVF contains components with "regenerative" properties, including stem cells that have shown promise for ameliorating specific disease conditions. This study is designed to evaluate joint pain and functionality changes in individuals with OA for up to 12 months following SVF treatment.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Fluent in English
  • Over the age of 18
  • Diagnosed with OA of the knee and/or hip
  • Scheduled for intravenous and intra-articular administrations of autologous SVF
  • Capable of understanding and willing to sign informed consent
  • Willing and able to complete brief phone interviews
  • Willing and able to complete online surveys
Exclusion Criteria
  • Co-morbidity with an autoimmune disorder
  • Pregnant, may become pregnant, or breastfeeding
  • Subjects for which baseline data is not available

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change from Baseline in Overall Knee Assessment Over the Course of a 12 Month Period as Measured by the Knee Injury and Osteoarthritis Outcome Score (KOOS LK 1.0)Baseline, 12 months

The change from baseline over the course of 12 months using participants' assessment of their knee and associated problems. Mean scores will be used for baseline (day 0) and all interviews up to month 12 (months 1, 3, 6, and 12). Answer options are graded on a 5 point Likert scale and each question gets a score from 0 to 4.

Change from Baseline in Overall Hip Assessment Over the Course of a 12 Month Period as Measured by the Hip Dysfunction and Osteoarthritis Outcome Score (HOOS LK 2.0)Baseline, 12 months

The change from baseline over the course of 12 months using participants' assessment of their hip and associated problems. Mean scores will be used for baseline (day 0) and all interviews up to month 12 (months 1, 3, 6, and 12). Answer options are graded on a 5 point Likert scale and each question gets a score from 0 to 4.

Secondary Outcome Measures
NameTimeMethod
Change from Baseline in Knee Pain at Month 12 as Measured by Participants Using the Knee Injury and Osteoarthritis Outcome Score (KOOS LK 1.0) The Pain SubscaleBaseline, Month 12

Participant assessment in the change in knee pain from baseline to month 12 using the KOOS pain subscale.

Change from Baseline in Function in Daily Living (ADL) at Month 12 as Measured by Participants Using the Hip Dysfunction and Osteoarthritis Outcome Score (HOOS LK 2.0) The ADL SubscaleBaseline, Month 12

Participant assessment in the change in function in daily living from baseline to month 12 using the HOOS ADL subscale.

Change from Baseline in Function in Sport and Recreation at Month 12 as Measured by Participants Using the Hip Dysfunction and Osteoarthritis Outcome Score (HOOS LK 2.0) The Sport/Rec SubscaleBaseline, Month 12

Participant assessment in the change in function in sport and recreation from baseline to month 12 using the HOOS sport/rec subscale.

Change from Baseline in Other Hip Symptoms at Month 12 as Measured by Participants Using the Hip Dysfunction and Osteoarthritis Outcome Score (HOOS LK 2.0) The Other Symptoms SubscaleBaseline, Month 12

Participant assessment in the change in other hip symptoms from baseline to month 12 using the HOOS other symptoms subscale.

Change from Baseline in Other Knee Symptoms at Month 12 as Measured by Participants Using the Knee Injury and Osteoarthritis Outcome Score (KOOS LK 1.0) The Other Symptoms SubscaleBaseline, Month 12

Participant assessment in the change in other knee symptoms from baseline to month 12 using the KOOS other symptoms subscale.

Change from Baseline in Function in Daily Living (ADL) at Month 12 as Measured by Participants Using the Knee Injury and Osteoarthritis Outcome Score (KOOS LK 1.0) The ADL SubscaleBaseline, Month 12

Participant assessment in the change in function in daily living from baseline to month 12 using the KOOS ADL subscale.

Change from Baseline in Hip Related Quality of Life (QOL) at Month 12 as Measured by Participants Using the Hip Dysfunction and Osteoarthritis Outcome Score (HOOS LK 2.0) The QOL SubscaleBaseline, Month 12

Participant assessment in the change in hip related quality of life from baseline to month 12 using the HOOS QOL subscale.

Change from Baseline in Function in Sport and Recreation at Month 12 as Measured by Participants Using the Knee Injury and Osteoarthritis Outcome Score (KOOS LK 1.0) The Sport/Rec SubscaleBaseline, Month 12

Participant assessment in the change in sport and recreation from baseline to month 12 using the KOOS sport/rec subscale.

Change from Baseline in Knee Related Quality of Life (QOL) at Month 12 as Measured by Participants Using the Knee Injury and Osteoarthritis Outcome Score (KOOS LK 1.0) The Knee Related Quality of Life SubscaleBaseline, Month 12

Participant assessment in the change in knee related quality of life from baseline to month 12 using the KOOS QOL subscale.

Change from Baseline in Hip Pain at Month 12 as Measured by Participants Using the Hip Dysfunction and Osteoarthritis Outcome Score (HOOS LK 2.0) The Pain SubscaleBaseline, Month 12

Participant assessment in the change in hip pain from baseline to month 12 using the HOOS pain subscale.

Trial Locations

Locations (1)

StemGenex

🇺🇸

San Diego, California, United States

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