Musculoskeletal Pain, Osteoarthritis
Conditions
Keywords
Platelet-rich Plasma, Cell-Derived Microparticles, Pain Management, Blood Platelets, Therapeutics, Inflammation, ThromboLUX, Dynamic Light Scattering
Brief summary
This is an observational study that evaluates the characteristics of Platelet Rich Plasma used in the therapy and treatment of musculoskeletal injuries and degenerative joint diseases. A sample of the PRP will be tested for platelet and microparticle content using dynamic light scattering to determine if there is a relationship between the composition and the treatment outcome.
Detailed description
An observational study that evaluates the characteristics of Platelet Rich Plasma used in the therapy and treatment of musculoskeletal and degenerative joint conditions. Patients enrolled in this study have already been assessed by the Principal Investigator and are schedule to receive treatment with Platelet Rich Plasma. Prior to the treatment patients will be asked to consent in the study where the composition of the PRP is to be evaluated. Consenting patients that meet inclusion/exclusion criteria will complete a pain score self-assessment prior to treatment. An autologous preparation of PRP sample will be made from the subject's whole blood. The subject will receive the PRP treatment and an excess portion of the PRP preparation will be tested for composition and the relative concentration of the constituents. The sample of the PRP will be tested using Dynamic Light Scattering (ThromboLUX System) to measure the constituents in PRP preparations prior to injection. PRP and whole blood (at physician's discretion) will be analyzed on a hematology analyzer. The testing work-flow does not alter the subject's standard of care. The physician will be blinded to the analytical results during the enrolment, treatment and patient follow-up phase of the study. Analytical results are not used in patient management decisions. Patient's response to the PRP treatment will be assessed at 3 and 6 weeks post injection. At these times, the clinical outcome of the treatment will be measured using a patient self -assessment (post-treatment pain scores). This study will test the hypothesis that PRP characteristics, such as platelet and microparticle content and composition can be predictive clinical outcome for PRP treatments. The clinical outcome will be evaluated by patient pre- and post-pain score assessment. This study aims to review clinical outcomes and compare these results against ThromboLUX and other test results. If the predictive value of platelet composition testing can be demonstrated, additional studies may be considered.
Interventions
None listed
Sponsors
LightIntegra Technology
University of British Columbia
Study design
Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
19 Years to 70 Years
Healthy volunteers
Yes
Inclusion criteria
* Are willing and able to give informed consent for participation in the study * Have a diagnosed injury/condition requiring PRP injection: patients with acute or chronic musculoskeletal injury, tendinopathy, or mild to moderate osteoarthritis of the knee * Are otherwise healthy * Agree to pre-treatment fasting (4 hours prior to treatment) * Agree to disclose medications taken in the last 2 weeks * Able (in the Investigators opinion) and willing to comply with all study requirements * Able to attend an on-site visit or provide information on your current status electronically, 3 and 6 weeks following the PRP injection * Have not previously received a PRP injection for your current injury
Exclusion criteria
* Unable to provide informed consent * Have any blood borne disease, currently or in the past * Have a systemic inflammatory disease, skin or joint infection, bleeding disorders, or compromised immune function * Have a known platelet abnormality or hematological disorder * Are not able or willing to share with the study team any medications taken in the last two weeks. * Taking anti-inflammatory medications or medications that interfere with clotting * Are female and are pregnant or breast feeding * Have inadequate venous access for drawing blood * Have any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the study, or may influence the result of the study, or the patients ability to participate in the study
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in pre- and post- pain score at 3 and 6 weeks | Up to 6 weeks after injection | The primary objective of the study is to test the hypothesis that the constituents in platelet-rich plasma (PRP) preparations, such as platelet and microparticle content and composition, can be correlated to the clinical outcome for PRP treatments. |
| The impact of microparticle content on pain scores | Up to 6 weeks after injection | The study will ascertain the capability of ThromboLUX microparticle assay results to correlate with the clinical outcome for PRP treatments when evaluated by patient pre- and post-pain score assessment. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Correlation of platelet count to ThromboLUX results | Up to 6 weeks after injection | Evaluation of PRP platelet count to clinical outcome and ThromboLUX data outputs |
| The use of dynamic light scattering (ThromboLUX) as a patient screening tool | Up to 6 weeks after injection | To verify the performance of the ThromboLUX instrument in a clinical setting by reviewing size and composition of constituents in PRP |
Countries
Canada
Outcome results
None listed