Phase 2
N=60
pAF for the Treatment of Osteoarthritis
Osteo Arthritis Knee
Bottom Line
View on ClinicalTrials.gov: NCT04886960 ↗Enrolled (actual)
60
Serious AEs
3.3%
Results posted
Mar 2026
Primary outcome: Primary: Repeat Allogeneic Intra-articular Injection Within 6 Months. — 6; 7 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- Amniotic Fluid Injection (Biological); Standard of Care (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of Utah
- Primary completion
- Jan 2025
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Repeat Allogeneic Intra-articular Injection Within 6 Months. |
6; 7 | — |
| SECONDARY Knee Injury and Osteoarthritis Outcome Score (KOOS) |
75; 50; 75; 69; 75; 58 | — |
| SECONDARY Visual Analog Scale for Pain (VAS Pain) |
3; 5 | — |
| SECONDARY Single Assessment Numerical Evaluation (SANE) |
61; 65 | — |
| SECONDARY Patient-Reported Outcome Measurement Information System (PROMIS) Physical Function Computer Adaptive Test (PF-CAT) |
48; 44 | — |
Summary
This is a Phase I/II Randomized Double-Blinded Standard of Care (Corticosteroid) vs. Sterile Amniotic Fluid for Osteoarthritis
Eligibility Criteria
Inclusion Criteria
- Patients who are between the ages of 18-70 years
- A confirmed diagnosis of knee osteoarthritis based on clinical and radiographic findings consistent with Kellgren-Lawrence Stage 2-3 disease
- Patients who have failed conservative treatment (e.g. steroid, activity modification, therapy, etc.) within 3 months
- Unilateral or bilateral chronic knee joint pain >4 months
- Patients who are able to ambulate (i.e. not wheelchair bound)
- Patient reported a typical pain of at least 4 out of 10 during the past week using VAS numeric pain scale (0-10)
- Patients who are of childbearing potential must agree to use adequate contraception for 90 days after study drug injection
Exclusion Criteria
- Subjects who have had a previous injection (i.e. steroid, platelet rich plasma, or other) within the last 3 months
- A focal chondral defect, defined by x-ray evaluation
- BMI >40 as defined by NIH Clinical Guidelines Body Mass Index
- Concurrent participation in another investigational trial involving systemic administration of agents (within the previous 30 days) or plans to participate in any other allogeneic stem cell therapy trial during the 12 month follow-up period
- Clinical suspicion of infection at injection site
- Any surgeries within 4 weeks, other than diagnostic surgery
- Insulin or self-reported non-insulin dependent diabetic evident of HgA1c ≥8% among known diabetics
- Unable to consent to an English Language Consent Form
- Frank mechanical issues (i.e. locking of the knee)
- Workman's Compensation cases
- Rheumatoid arthritis
- Patients with a known allergy to local anesthetics or components of the study drug (pAF or steroid injection)
- Patients with vascular claudication or neurologic disorders affecting the index lower limb
- Patients with inflammatory arthropathies or connective tissue disorders; or
- Patients with known alcohol or drug abuse or dependence, recreational use of illicit drug or prescription medications, or have used medical marijuana within 7 days of study enrollment
- Patients with history of active cancer/malignancy within 2 years of screening, apart from adequately treated basal cell or squamous cell carcinoma of the skin not associated with the target knee
- Women who are nursing or pregnant
- Patients of childbearing potential who are unwilling to use adequate contraception for 90 days after study drug injection
Data sourced from ClinicalTrials.gov (NCT04886960). 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.