Expired Study
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Richmond, Virginia 23224


Purpose:

The purpose of this study is to evaluate the affect that platelet rich plasma has on the molecular an cellular functioning of the knee joint.


Study summary:

In this study 18 subjects with mild to moderate symptomatic knee osteoarthritis will be recruited per an IRB approved protocol with explicit inclusion and exclusion criteria. Subjects who are enrolled and meet all criteria will be blinded and randomized (2:1) to receive Platelet Rich Plasma or normal saline "control". Prior to the intervention, a synovial fluid aspiration will occur. At follow up number one (approximately 10 days from baseline) a repeat aspiration will occur and a differential analysis of the molecular and biochemical effects will be undertaken; this data will serve as the primary outcome measures. This data will be correlated to clinical and imaging outcome measures which will be secondary outcome measures completed at baseline and intermittently throughout the study. The duration of the study is one year.


Criteria:

Inclusion Criteria: 1. Early/Mild to Moderate Stage knee osteoarthritis (KOA), as determined by Kellgren-Lawrence Grade 2 to 3 on PA standing radiograph within the past three months; - A prospective subject who has a diagnosis of non-end stage KOA (i.e., a potential study candidate) and expresses interest in participating but has no XRAY within the specified time-period will be sent for a fresh XRAY. This XRAY will be read by a radiologist & be paid for by the study. 2. >=40 years of age; 3. Average 100-point VAS score of >50, on average, within the past 3 months*, with KOA felt to be the primary contributor to pain. - Alternate 10-point scales with pain scores averaging >5 may be considered if the prospective subject also completes a VAS with score >50 at screening. 4. Exam consistent with KOA being primary etiology of pain; 5. No signs of inflammatory arthropathy in medical record, history or physical examination; 6. A >3 millimeter intra-articular (IA) effusion present on ultrasound evaluation. 7. [If a chronic liver or renal disease patient, evidence of stable disease over/within the past six months, else exclusion.] 8. Veteran receiving care at McGuire VAMC. Exclusion Criteria: 1. Morbid obesity (BMI >40); 2. Poorly controlled diabetes (hemoglobin A1C > 7.5 or fasting blood glucose of >200) in last 6 months; 3. Ipsilateral knee surgery, trauma within last 6 months, or corticosteroid injection within 3 months. 4. 4. History of inflammatory arthropathy (RA, SLE or crystalline arthritis of the knee)**; 5. Any rheumatoid arthritis or gout diagnosis is exclusionary. 6. Current infection of the affected joint or any other uncontrolled or untreated active infection. 7. Moderate to severe anemia (hemoglobin < 11 g/dl) or thrombocytopenia (platelet count < 100,000); Hemoglobin >17 g/dl or <11 g/dl and/or platelet counts >500,000 or <100,000 platelets/μl. - [CBC obtained within 6 months will be required, even if obtained at initial screening visit.] 8. Individuals on dialysis, with liver failure, or uncontrolled renal or liver disease are excluded. - In those with chronic renal or liver disease, documentation of stable disease within the most recent 6 months will be required. 9. Individuals on a therapeutic anticoagulant (e.g., Warfarin, Dabigatran, Enoxaparin) and those with a history of coagulopathy are excluded. - Per standard clinical practice, subjects on anti-platelet therapy are not excluded. 10. Pregnancy or breast-feeding; - Female subjects of child-bearing potential must have a negative pregnancy screen prior to enrollment. - Female subjects of child-bearing potential must confirm they are not actively breast-feeding prior to enrollment. 11. Current illicit drug abuse / active alcohol abuse (i.e, Current substance abuse); 12. Uncontrolled psychiatric disorder; 13. Lack of transportation (i.e., to get to/from appointments at VAMC) and/or willingness to attend study appointments (screening/consent, Intervention, Day10-follow-up, Month-6 follow-up, and then visits over-the-phone / in-person / or via Telehealth for Month-3 and Month-12; 14. Advanced or currently active cancer. 15. Blood disorders (such as Sickle Cell Anemia, TTP, others) 16. Vulnerable populations: Individuals incapable of making informed decisions will not be enrolled, nor will those under some form of incarceration.


Study is Available At:


Original ID:

IRB #01979/FDA IDE#15944


NCT ID:

NCT02468492


Secondary ID:


Study Acronym:


Brief Title:

Pilot Synovial Fluid Molecular/Stem Cell Response to PRP in Knee Osteoarthritis: Clinical & Imaging Outcome Correlation


Official Title:

Synovial Fluid Biomarker and Mesenchymal Stem Cell Response to PRP in Knee Osteoarthritis With Clinical and Imaging Outcome Correlation: Proof of Concept Study


Overall Status:

Completed


Study Phase:

N/A


Genders:

N/A


Minimum Age:

40 Years


Maximum Age:

N/A


Quick Facts

Healthy Volunteers
Oversight Has DMC
Study Is FDA Regulated
Study Is Section 801
Has Expanded Access

Study Source:

Hunter Holmes Mcguire Veteran Affairs Medical Center


Oversight Authority:

United States: Food and Drug Administration


Reasons Why Stopped:


Study Type:

Interventional


Study Design:


Number of Arms:

2


Number of Groups:

0


Total Enrollment:

18


Enrollment Type:

Actual


Overall Contact Information

Official Name:Lance L Goetz, MD
Principal Investigator
Hunter Holmes McGuire VAMC

Study Dates

Start Date:September 2014
Completion Date:November 2015
Completion Type:Actual
Primary Completion Date:November 2015
Primary Completion Type:Actual
Verification Date:August 2017
Last Changed Date:August 13, 2017
First Received Date:May 31, 2015

Study Outcomes

Outcome Type:Secondary Outcome
Measure:Imaging Outcomes
Time Frame:6 months
Safety Issues:False
Description:Evaluation for change in joint space width using knee radiographs at baseline and 6 month follow up.
Outcome Type:Secondary Outcome
Measure:Clinical Outcomes
Time Frame:1 year
Safety Issues:False
Description:Evaluation for change in pain level via VAS and WOMAC at baseline and follow up.
Outcome Type:Primary Outcome
Measure:Biochemical Molecular Outcomes
Time Frame:Baseline and 10 day follow up
Safety Issues:False
Description:Evaluate for change in biochemical molecular milieu temporal response after PRP injection or normal saline (control) compared to baseline, as measured by multiplex suspension array technology.

Study Interventions

Intervention Type:Biological
Name:Platelet Rich Plasma
Description:Platelet rich plasma injection into knee versus placebo (saline) injection.
Arm Name:Platelet Rich Plasma
Other Name:Platelet Concentrate
Intervention Type:Other
Name:Normal Saline
Description:Platelet rich plasma injection into knee versus placebo (saline) injection.
Arm Name:Normal Saline

Study Arms

Study Arm Type:Other
Arm Name:Normal Saline
Description:Approximately 5mL of intraarticular normal saline once at baseline
Study Arm Type:Experimental
Arm Name:Platelet Rich Plasma
Description:Approximately 5mL of intraarticular PRP once at baseline

Study Agencies

Agency Class:U.S. Fed
Agency Type:Lead Sponsor
Agency Name:Hunter Holmes Mcguire Veteran Affairs Medical Center
Agency Class:Other
Agency Type:Collaborator
Agency Name:Foundation for Physical Medicine and Rehabilitation

Sample and Retention Information

There are no available Sample and Retention Information

Study References

There are no available Study References

Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

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