N/A
N=86
Randomized Evaluation of the Efficacy of Synvisc-One® for the Treatment of Patellofemoral Chondromalacia
Chondromalacia Patella · Patellofemoral Pain Syndrome
Bottom Line
View on ClinicalTrials.gov: NCT01771952 ↗Enrolled (actual)
86
Serious AEs
0.0%
Results posted
Sep 2020
Primary outcome: Primary: Knee Pain During a Single Leg Squat — 5.6; 5.2; 4.1; 3.4 units on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Synvisc-One™ (Device); Sham Treatment (Other)
- Age
- Pediatric, Adult · 15+ yrs
- Sex
- All
- Sponsor
- University of Virginia
- Primary completion
- Oct 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Knee Pain During a Single Leg Squat |
5.6; 5.2; 4.1; 3.4; 3.6; 2.2 | — |
| SECONDARY KOOS: Patient Reported Knee Function |
63.5; 64.9; 68.9; 79.9; 70.7; 79.9 | — |
| SECONDARY Quadriceps Muscle Function |
1.63; 1.84; 1.77; 1.84; 1.45; 1.68 | — |
Summary
The purpose of this study is to determine how safe a knee injection called Synvisc-One® is in patients with a condition called chondromalacia patella and how well in works in treating the condition.
Chondromalacia patella is a common cause of kneecap pain or front knee pain. Often called "Runner's Knee," this condition often affects young, otherwise healthy individuals.
Chondromalacia is due to irritation of the undersurface of the kneecap. The undersurface of the kneecap, or patella, is covered with a layer of smooth cartilage. This cartilage normally glides effortlessly across the knee during bending of the joint. In some individuals, the cartilage on the undersurface of the knee cap becomes irritated and soft, resulting in pain. Potential treatments for this condition include rest, injections (numbing or anti-inflammatory medications to reduce swelling and pain), and/or guided strengthening exercises which may help reduce pain.
Other Treatments are being evaluated. This study is about Synvisc-One® an experimental device that has been approved by the Food and Drug Administration (FDA) for the treatment of pain in osteoarthritis (OA) of the knee in patients who have failed to respond to treatments that do not involve drugs or surgery and simple pain medication such as acetaminophen. Synvisc-One® is a gel-like substance that, when injected into a joint, acts to lubricate and cushion the joint. Synvisc-One® is made from hyaluronan, which is a molecule that is found normally in joint fluid.
Synvisc-One® has not been proven to be safe or helpful in patients with chondromalacia patella (cartilage irritation or softening of the undersurface of the 'knee cap'). So far, this drug/device has been given to over 10,000 people who have knee pain (due to osteoarthritis) and has been proven safe and effective in patients with moderate to severe pain due to knee joint osteoarthritis.
Eligibility Criteria
Inclusion Criteria
- Age at time of randomization: 18-45 years
- Clinical diagnosis of anterior knee pain
- X-ray showing no fracture or osteoarthritis
- >4 out of 10 on a visual analog scale and/or Knee & Osteoarthritis Outcome Score (KOOS) 40
- Prior surgery in the knees (excludes debridement only procedures)
- Clinical evidence of hip disease
- Any form of inflammatory arthritis ( e.g. RA, gout, pseudogout, lupus, etc)
- Significant co-morbid conditions as determined by the investigator
- Willing to refrain from chiropractic treatment or acupuncture during the study
- Any other intra-articular knee joint injection during the study
- Kellgren Lawrence grade osteoarthritis of II, III or IV
Data sourced from ClinicalTrials.gov (NCT01771952). 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.