Injections of FloGraft Therapy, Autologous Stem Cells, or Platelet Rich Plasma for the Treatment of Degenerative Joint Pain



Status:Not yet recruiting
Conditions:Arthritis, Osteoarthritis (OA), Rheumatoid Arthritis
Therapuetic Areas:Rheumatology
Healthy:No
Age Range:18 - Any
Updated:4/2/2016
Start Date:January 2014
Contact:Edward L Swing, PhD
Email:TedS@arizonapain.com
Phone:480-245-6138

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Outcomes of Single Injections of FloGraft Therapy, Autologous Stem Cells, or Platelet Rich Plasma for the Treatment of Pain in the Lumbar Facet Joints, Sacroiliac Joints, Upper Extremity Joints, and Lower Extremity Joints

This study will assess the outcomes of three currently available regenerative treatments
(FloGraft, autologous stem cell therapy, platelet rich plasma therapy) for painful
degenerative conditions of the joints. Patients receiving one these treatments will be
assessed before the treatment procedure and followed up at four points over the six months
after their procedure. Patients' pain, quality of life, and pain medication use at follow up
will be compared to baseline levels. The investigators hypothesize that all three treatments
will be effective in reducing pain, improving quality of life, and reducing pain medication
usage.

This is an open-label, non-randomized study assessing the efficacy of three potentially
regenerative treatments for degenerative conditions of the joints of the lower back (facet,
sacroiliac), upper extremities (e.g., shoulder), and lower extremities (e.g., hip, knee).
These treatments are:

1. A single injection of Applied Biologics' FloGraftTM.

2. A single injection of autologous bone marrow derived stem cells.

3. A single injection of platelet rich plasma.

Subjects will be assessed prior to treatment for their level of pain, quality of life, and
pain medication usage. Subjects will be followed up at 4 weeks, 8 weeks, 12 weeks, and 24
weeks after treatment. At each of these follow up visits, pain, quality of life, and pain
medication usage will be assessed.

The investigators hypothesize that all three treatment groups will experience reduced pain,
improved quality of life, and reduced pain medication usage at follow up.

Inclusion Criteria:

- Age 18 or older,

- Ability to complete follow-up visits,

- Able to understand the study protocol and provide consent,

- Significant pain (average pain in the past month greater than or equal to 5, from
0-10),

- Pain lasting at least 3 months,

- Pain associated with one of the following conditions: lumbar facet degeneration, - OR
-degenerative condition causing upper extremity joint pain, - OR - degenerative
condition causing lower extremity joint pain.

Exclusion Criteria:

- Current litigation or worker's compensation claim,

- Unstable pain medication dosage,

- Previous surgery at the affected site,

- Injections at the affected site within the past 6 months,

- Uncontrolled psychiatric condition,

- Pregnancy or lactating in women,

- History of adverse reactions to local anesthetic
We found this trial at
1
site
Scottsdale, Arizona 85258
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Scottsdale, AZ
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