Clinical Trial Finder

Inclusion Criteria:

• - patients age 18 to 35 years with closed growth plates as visualized on plain radiographs who participate in cutting and pivoting activities.

• - we will enroll an equal number of men and women in each treatment group (16 total per group; 8 men, 8 women).

• - study participants must have an MRI-confirmed ACL injury within 2 weeks of presentation.

• - must elect to undergo bone-patellar tendon-bone (BTB) autograft ACL reconstruction within 45 days of injury.

• - no clinical or MRI evidence of posterior cruciate ligament injury.

• - no more than grade 1 medial collateral ligament injury.

• - no concurrent posterolateral corner injury to the ipsilateral knee.

Exclusion Criteria:

• - injury occurring more than 2 weeks prior to enrollment.

• - previous ipsilateral knee injury.

• - multi-ligamentous knee injury.

• - pre-existing or concurrent grade 3 or 4 chondral (cartilage) injuries.

• - previous ipsilateral knee surgery (meniscus tear, ACL tear, chondral injury, etc.) - of note, concurrent acute meniscus injury is NOT an exclusion criteria.

• - active infection.

• - known allergy or adverse reaction to anakinra.

• - intra-articular cortisone injection into either knee within 3 months of injury.

• - prior exposure to IL-1Ra.

• - participation in another clinical drug trial within the 4 weeks before injury.

• - history of any coagulopathy or current anti-coagulation therapy.

• - current malignancy.

• - current inflammatory/rheumatologic disease.

• - current immune-compromised state.

- current renal failure

After appropriate IRB approval at total of 32 active patients who meet the inclusion criteria listed above will be randomized into three treatment groups. A total of 16 patient will be in Group 1 and 16 patients will be in Group 2. An equal number of males and females in each treatment group (8 males, 8 females).

• - Group 1 (n = 16) will undergo arthrocentesis of the knee hemarthrosis at the time of presentation in clinic within 2 weeks from the date of knee injury.

Following aspiration of the knee joint hemarthrosis, an injection of approximately 5 milliliters (mls) of 0.9% sodium chloride solution (sterile saline) will be administered as a placebo control. In addition, a second aspiration of knee joint fluid and injection of sterile saline into the injured knee joint will be performed 3-5 days after initial injection.

• - Group 2 (n=16) will receive arthrocentesis as described in group 1, however, following arthrocentesis patients will then receive an intra-articular knee injection of anakinra (150mg, ~1.5mls) plus sterile saline (~3.5mls) at the time of initial enrollment in the study as well as a second knee joint aspiration and intra-articular knee injection of anakinra (150mg, ~5mls) plus sterile saline (~3.5mls) at 3 to 5 days after the initial injection.

All participants will undergo two knee aspiration and injection procedures prior to surgery. The injections will occur after the arthrocentesis procedure, which removes some of the hemarthrosis associated with acute ACL injury. To minimize pain and discomfort the same needle stick will be used to aspirate the hemarthrosis and to inject the saline or anakinra depending on the patient's treatment group. The second knee arthrocentesis and injection in each patient will also be performed at 3 to 5 days after initial injection. An additional arthrocentesis procedure will be performed at the time of surgery. Ultrasound guidance will be used whenever feasible. Participants in both treatment groups will undergo pre-operative collection of urine and knee joint fluid as described above. These time points include: i) at the time of enrollment into the study (within 2 weeks of injury), ii) 3-5 days after initial injection, iii) on the day of surgery (within 45 days of injury). Of note, if no fluid is able to be aspirated from the knee joint after the initial aspiration, then joint fluid may not be obtained. In addition, urine and knee joint fluid collection will be performed at the initial post-operative visit (approximately 8-10 days after surgery) followed by collection of urine alone at 3, 6, 9, 12 and 24 months post-operatively in all treatment groups. Urine and arthrocentesis samples will be analyzed for the presence of inflammatory cytokines and cartilage breakdown biomarkers (Aim 1) according to Osteoarthritis Research Society International guidelines (see cytokine and biomarker assays section below for further details). Given, that multiple studies have demonstrated resolution of cytokine abnormalities by 2 to 4 weeks after ACL injury, urine assessments of cytokine assays (IL-1, etc.) will not be conducted beyond 3 months post-operatively. However, ELISAs for cartilage biomarkers will be performed on urine collected at each time point throughout the duration of the study. Validated patient reported outcome assessments (KOOS, VAS and PROMIS) will be completed at initial presentation as well as at 6, 9, 12 and 24 month post-operatively. Participants both groups will be followed longitudinally with repeated MR imaging that includes cartilage-sensitive T1rho sequences when available. Whenever possible, the study team will obtain T1rho magnetic resonance (MR) image sequences of the injured knee within 3 weeks of patient injury. Due to time constraints and research MRI scanner availability T1rho magnetic resonance (MR) image sequences are currently not always able to be obtained in the short time window between patient injury and patient enrollment into the study. In addition, given the social distancing recommendations associated with the ongoing COVID-19 pandemic, reducing patient exposure to the confined indoor spaces on the UCLA medical campus during a global pandemic would be ideal. The most important follow up time points for assessment of the T1rho MRI outcome measure are at 1 year and 2 years post-operatively. An alternative to obtaining baseline T1rho images of the patient's injured knee is to image, the patients' contralateral knee as a control for comparison. Thus, T1rho MR images of study patients will be acquired at 1 year and 2 years post-operatively (Aim 3). Each patient's contralateral knee will serve as an internal control for comparison as needed. For further imaging assessment details please refer to the "Imaging" section below. This study will be a single-blinded design and all aspects of the study design will be disclosed to subjects during the informed consent process. Given that anakinra needs to be ordered by the physician from the pharmacy on the day of injection, the physician performing the injection will not be blinded to which patients receive anakinra treatments. However, the patients will be blinded regarding which treatment they receive. All patients will receive injections of the same volume and using the same type of needle and syringe. In addition, the radiologist interpreting the MRI studies, including T1rho images, will be blinded to which treatment the patients receive. The physician administering the injections into the joint will not be involved in interpreting the MRI findings and will not be present when subjects complete the patient-reported outcome measures. In addition, the synovial fluid and urine biomarker data will be analyzed in a coded fashion by a blinded laboratory technician in conjunction with a statistician to avoid bias in the statistical analysis.

Arms

Placebo Comparator: Control

Subjects will receive two injections of sterile saline after ACL injury, prior to surgery

Active Comparator: Two doses Anakinra

Subjects will receive two injections of anakinra after ACL injury, prior to surgery

Interventions

Drug: - Anakinra injection

anakinra 150mg in 5milliliters of sterile saline will be injected into the knee joint

Procedure: - sterile saline injection

5 milliliters of sterile saline will be injected into the knee joint