- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02241408
Outcomes Data of Adipose Stem Cells to Treat Osteoarthritis
August 28, 2018 updated by: StemGenex
Autologous Adipose Stromal Vascular Fraction Outcomes in Osteoarthritis Research Study
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.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
100
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
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California
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San Diego, California, United States, 92121
- Recruiting
- StemGenex
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Contact:
- Phone Number: 855-742-7836
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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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Community Sample
Description
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 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
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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)
Time Frame: 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.
|
Baseline, 12 months
|
|
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)
Time Frame: 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.
|
Baseline, 12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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 Subscale
Time Frame: Baseline, Month 12
|
Participant assessment in the change in knee pain from baseline to month 12 using the KOOS pain subscale.
|
Baseline, Month 12
|
|
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 Subscale
Time Frame: Baseline, Month 12
|
Participant assessment in the change in function in daily living from baseline to month 12 using the KOOS ADL subscale.
|
Baseline, Month 12
|
|
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 Subscale
Time Frame: Baseline, Month 12
|
Participant assessment in the change in sport and recreation from baseline to month 12 using the KOOS sport/rec subscale.
|
Baseline, Month 12
|
|
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 Subscale
Time Frame: Baseline, Month 12
|
Participant assessment in the change in knee related quality of life from baseline to month 12 using the KOOS QOL subscale.
|
Baseline, Month 12
|
|
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 Subscale
Time Frame: Baseline, Month 12
|
Participant assessment in the change in other knee symptoms from baseline to month 12 using the KOOS other symptoms subscale.
|
Baseline, Month 12
|
|
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 Subscale
Time Frame: Baseline, Month 12
|
Participant assessment in the change in hip pain from baseline to month 12 using the HOOS pain subscale.
|
Baseline, Month 12
|
|
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 Subscale
Time Frame: Baseline, Month 12
|
Participant assessment in the change in function in daily living from baseline to month 12 using the HOOS ADL subscale.
|
Baseline, Month 12
|
|
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 Subscale
Time Frame: Baseline, Month 12
|
Participant assessment in the change in function in sport and recreation from baseline to month 12 using the HOOS sport/rec subscale.
|
Baseline, Month 12
|
|
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 Subscale
Time Frame: Baseline, Month 12
|
Participant assessment in the change in hip related quality of life from baseline to month 12 using the HOOS QOL subscale.
|
Baseline, Month 12
|
|
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 Subscale
Time Frame: Baseline, Month 12
|
Participant assessment in the change in other hip symptoms from baseline to month 12 using the HOOS other symptoms subscale.
|
Baseline, Month 12
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
September 1, 2014
Primary Completion (Anticipated)
September 1, 2019
Study Completion (Anticipated)
September 1, 2019
Study Registration Dates
First Submitted
September 13, 2014
First Submitted That Met QC Criteria
September 13, 2014
First Posted (Estimate)
September 16, 2014
Study Record Updates
Last Update Posted (Actual)
August 31, 2018
Last Update Submitted That Met QC Criteria
August 28, 2018
Last Verified
August 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SVF01OA
- ASCOA-01
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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