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N/A N=90 Randomized Quadruple-blind Treatment

Autologous Conditioned Plasma (ACP) Intra-articular (IA) Injections for Knee Osteoarthritis (OA)

Osteoarthritis

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

OutcomeResultp-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.
View full record on ClinicalTrials.gov →

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.

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