Osteoarthritis, Knee
Conditions
Brief summary
Safety & Efficacy of FloGraft (Micronized Human Amnion Chorion Membrane)® in Adults With Pain Due to Osteoarthritis of the Knee.
Interventions
DRUGmHACMb
Active ingredient
OTHERplacebo
inactive ingredient
Sponsors
Applied Biologics, LLC
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
30 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Able to provide written informed consent to participate in the study. * Willing and able to participate in all procedures and follow-up evaluations necessary to complete the study. * Subject is 30 years or older. * Moderate OA pain (rating of at least 20mm on the VAS) assessed at Baseline. * Moderate to moderately-severe OA pain in the index knee (rating of at least 1.5 on the WOMAC Index 3.1 5-point Likert Pain Subscale) assessed at Baseline. * Must be ambulatory. * No analgesia (including acetaminophen \[paracetamol\]) taken 12 hours prior to an efficacy measure.
Exclusion criteria
* Subject has active infection at the injection site. * Subject has rheumatoid arthritis, psoriatic arthritis, or have been diagnosed with any other auto-immune disorders that could be the cause of their knee pain. * BMI greater than 40 kg/m2. * Subject has received an intra-articular hyaluronic acid (HA) injection for the treatment of OA of the target knee within 3 months prior to screening. * Subject has received an intra-articular amniotic fluid, amniotic membrane or amniotic fluid/membrane combination injection for the treatment of OA of the target knee within 3 months prior to screening. * Subject has received a steroid, bone marrow aspirate concentrate (BMAC) or platelet rich plasma (PRP) injection for the treatment of OA of the target knee within 3 months prior to screening. * Subject has had major surgery, arthroplasty or arthroscopy in the target knee within 26 weeks of treatment or plans to have surgery in the target knee within 180 days of treatment. * Subject is pregnant or plans to become pregnant within 180 days of treatment. * Subject has used an investigational drug, device or biologic within 12 weeks prior to treatment. * Subject has any significant medical condition that, in the opinion of the Investigator, would interfere with protocol evaluation and participation. * Subject is currently taking anticoagulant therapy (excluding Plavix or Aspirin). * Diagnosis of gout in the past 6 month. * Major injury to the target knee within the 12 months prior to the screening. * Severe hip osteoarthritis ipsilateral to the target knee. * Any pain that could interfere with the assessment of the target knee pain (e.g. pain in any other part of the lower extremities, pain radiating to the knee).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Visual Analogue Scale (VAS) | 3 Months | Decreased Pain Level |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Western Ontario and McMaster Universities Arthritis Index (WOMAC®) osteoarthritis Index 3.1. | 3 Months | Decrease in pain, stiffness, and physical functioning of the joints. |
Countries
United States
Contacts
Primary ContactSamantha Montgomery
Outcome results
None listed