N/A
N=90
Autologous Conditioned Plasma (ACP) Intra-articular (IA) Injections for Knee Osteoarthritis (OA)
Osteoarthritis
Bottom Line
View on ClinicalTrials.gov: NCT02713542 ↗Enrolled (actual)
90
Serious AEs
0.0%
Results posted
Aug 2019
Primary outcome: Primary: Pain Scores Measured by Western Ontario and McMaster Universities Index (WOMAC) Survey — 3.98; 5.54 units on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- ACP (Device); Placebo (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Arthrex, Inc.
- Primary completion
- Jul 2018
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Pain Scores Measured by Western Ontario and McMaster Universities Index (WOMAC) Survey |
3.98; 5.54 | — |
Summary
This study is primarily investigating the effectiveness of Autologous Conditioned Plasma (ACP) Intra-articular (IA) in patients with Osteoarthritis (OA) in the knee.
Eligibility Criteria
Inclusion Criteria
- The subject is 18 to 70 years of age.
- The subject presents with complaints of continued pain of primary knee for at least 6 weeks.
- The subject has documented radiographs evidence of Osteoarthritis (OA) in the tibio-femoral or patella-femoral compartment of the target knee (Kellgren-Lawrence Grades II-III), using radiographs performed within 24 weeks of screening.
- The subject has a WOMAC pain score of at least 8 out of 20 and at least moderate pain (a score of 2) for at least 2 questions on activities
Exclusion Criteria
- Grade I and IV on the knee Kellgren-Lawrence grading scale
- Subject has clinically 3+ effusion of the target knee (stroke test grading system).
- Subject has significant (> 10⁰) valgus or varus deformities as evidenced by standard of care X-ray.
- Subject has had systemic or IA injection of corticosteroids in any joint within three months prior to screening.
- Viscosupplementation in any joint in the past six months.
- Subject has an increased risk for post- procedure bleeding (e.g., bleeding disorder or taking anticoagulants except low-dose aspirin).
- Subject had prior open surgery on the target knee within 12 months or knee arthroscopy within 6 months
- Subject has inflammatory disease of either knee other than OA.
- Subject with underlying medical conditions that could interfere with the evaluation of the outcome.
- Subject with positive pregnancy test, or breast feeding.
- Subject with plans to participate in other clinical trial involving medical or surgical intervention in the next 12 months.
- Subject with any condition (including cognitive impairment) that, in the opinion of the investigator, might interfere with the evaluation of the study objectives.
- Subject has rheumatoid arthritis or gout
- Subject has a history of or a current infection at the affected joint.
- Subject with plans to undergo any elective orthopedic surgery in the next 12 months.
- Subject requires pain management therapy (with the exception of acetaminophen) not related to the target knee.
Data sourced from ClinicalTrials.gov (NCT02713542). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.