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Failed to enroll any patients despite study modifications
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| Name | Class |
|---|---|
| Forest Laboratories | INDUSTRY |
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This is a study to evaluate the efficacy of Ceftaroline in the treatment of bone and joint infections.
Study evaluates the efficacy of Ceftaroline 600mg IV every 8 hours for the treatment of acute osteomyelitis and/or infected joints.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Acute Osteomyelitis - Non MRSA | Experimental | For treatment of Acute osteomyelitis (< 6 months duration) Non MRSA isolate- Ceftaroline 600 MG (milligram) IV (intra-venous) every 8 hours for 6 weeks. |
|
| Acute osteomyelitis MRSA isolate | Experimental | For treatment of Acute osteomyelitis (< 6 months duration) MRSA isolate- Ceftaroline 600 MG IV every 8 hours for 8 weeks. |
|
| Prosthetic joint infection | Experimental | For treatment of prosthetic joint infection Ceftaroline 600 mg IV every 8 hours for 6 weeks. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ceftaroline | Drug | The duration of treatment will vary based on type of infection (acute osteomyelitis or joint infection) and if MRSA positive or negative. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Sustained clinical remission from the treated osteoarticular infection | Sustained clinical remission is defined by the absence of either clinical or microbiological evidence of failure at 1 year after study drug completion, in patients who complete the protocol's antibiotic regimen(s) and did not require subsequent antibiotics for their osteoarticular infection beyond the protocol prescribed regimen. | 1 year after study drug completion |
| Measure | Description | Time Frame |
|---|---|---|
| Initial clinical success from the treated osteoarticular infection | Initial clinical success will be measured by the agreement of the Infectious disease consultant and Orthopedic surgeon that the patient has had a positive response to therapy. Success will be measured by decrease of CRP (C reactive protein) by 50% from baseline if initially elevated, no evidence of drainage, sinus tract formation or infection related bone instability. Follow up cultures, if available are negative for originally isolated organism. In patients with prothetic joints no new warmth, tenderness or inflammation. |
| Measure | Description | Time Frame |
|---|---|---|
| Number of participants with defined symptoms, signs and lab values as markers of safety and tolerance. | Symptoms will be assessed daily by study team while patient is hospitalized and reviewed weekly by investigator while the patient is receiving study drug. Specific symptoms will include fever, chills, rash, nausea. diarrhea, abdominal pain, pain at the surgical/infection site, vertigo, shortness of breath, hives or other rash. A baseline physical will be performed on enrollment and repeated each week at follow up visits. Labs will checked at baseline, then daily through hospitalization and then weekly. If patient develops persistent diarrhea a stool test for C. Diff PCR (polymerase chain reaction) will be performed. |
Inclusion Criteria:
Adults > 18 years of age with the following osteoarticular infections:
Infected prosthetic knee or hip (first or second episode) with 2 stage procedure planned.
Criteria for infected joint:
Acute osteomyelitis of an extremity Criteria for acute osteomyelitis (all 4 needed)
Exclusion criteria:
Immunocompromised hosts:
Diabetic foot infections
Osteomyelitis in association with decubitus ulcers
Vertebral osteomyelitis/spinal epidural abscess
Septic bursitis
Gonococcal arthritis
Ceftaroline nonsusceptible organisms isolated from bone, joint or blood.
Infected external fixation devices
Calculated creatinine clearance < 50 mL/min at baseline
History of severe penicillin/B lactam allergy (ID to evaluate)
Intravenous drug use - lifetime exclusion
Patients with a nail puncture wound to foot
Patients at high risk for MDR (multidrug resistant) Gram negative organisms
Please note the use of antibiotic containing cement is not exclusion, as it represents standard of care in some of the infections to be studied
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| Name | Affiliation | Role |
|---|---|---|
| Mark R. Wallace, MD | Orlando Health | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Orlando Regional Medical Center | Orlando | Florida | 32806 | United States |
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| ID | Term |
|---|---|
| D010019 | Osteomyelitis |
| ID | Term |
|---|---|
| D001850 | Bone Diseases, Infectious |
| D007239 | Infections |
| D001847 | Bone Diseases |
| D009140 | Musculoskeletal Diseases |
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| ID | Term |
|---|---|
| D000097583 | Ceftaroline |
| D007267 | Injections |
| ID | Term |
|---|---|
| D002511 | Cephalosporins |
| D047090 | beta-Lactams |
| D007769 | Lactams |
| D000577 | Amides |
| D009930 |
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| 30 days after conclusion of study antibiotic |
| Day one through one year after completion of study drug. |
| Organic Chemicals |
| D013843 | Thiazines |
| D013457 | Sulfur Compounds |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |
| D004333 | Drug Administration Routes |
| D004358 | Drug Therapy |
| D013812 | Therapeutics |