This is a pivotal, prospective, multi-center, randomized, concurrent control, patient and assessor-blinded study with two arms: a treatment arm (where subjects will be treated with the EP Granules with Tobramycin investigational device in the 1st stage of a staged revision for periprosthetic joint infection (PJIs), and a control arm (where subjects are treated with the standard-of-care revision for infected PJIs).
This is a pivotal, prospective, multi-center, randomized, concurrent control, patient and assessor-blinded study to demonstrate superiority of new bone growth and a reduction in recurring infections, and thereby improve outcomes for patients undergoing a staged revision for periprosthetic joint infections (PJIs). The standard of care for treatment of PJIs typically involves either a 2-stage revision or 1.5 stage revision which entails loss of bone stock resulting from debridement of infected bone in Stage 1. In the Stage 2 procedure, surgeons use metal cones to make up for this bone loss and better support the revision implant. Inadequate bone growth could result in gaps at the the voids below the level of the cortical bone, resulting in regions with no contact with the revision implant or cement mantle. Such gaps could result in dead-space regions, and zones without new bone growth required to support the revision implant. Both deficiencies affect long-term survival of the revision implant. The study has two arms: a treatment arm (where subjects will be treated with the EP Granules with Tobramycin investigational device in the 1st stage of the staged surgical treatment, and a control arm where subjects are treated with the standard-of-care staged surgical treatment for infected PJIs. Outcomes are demonstration of new bone growth and reduction of recurrent infections.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
204
EP Granules with Tobramycin is a Ca-salt resorbable intended for orthopedic applications as a bone void filler for bone gaps or voids and in cases where risk of post-operative infection is high, such as the first stage of a 2-stage or 1.5 stage revision of an infected total joint.
Voids are left empty
University of Southern California
Los Angeles, California, United States
RECRUITINGEndeavor Health Skokie Hospital
Skokie, Illinois, United States
A single composite outcome of new bone growth and reduction in infection rates, with absence of serious device related adverse events.
A\] New bone growth observed in voids at 12 months versus pre-op stage 1 and B\] Absence of infection at 24 months versus pre-op stage 1 surgery.
Time frame: 24 months after stage 1 surgery
Absence of serious device related adverse events requiring re- operation
A serious device related adverse event requiring re-operation * Success = no adverse event occurs * Failure = adverse event occurs
Time frame: 24 months after stage 1 surgery
Secondary outcome: patient reported quality of life.
SF-12 or PROMIS -10 score
Time frame: 12 months after stage 1 surgery
Secondary outcome: AKSS Score
1\. AKSS Pain and Function Scores
Time frame: 12 months after stage 1 surgery
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RECRUITINGMassachusetts General Hospital
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NOT_YET_RECRUITINGBrigham & Womens Hospital
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RECRUITINGU Michigan Medical Center
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RECRUITINGHospital for Special Surgery
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RECRUITINGSanford South University Medical Center
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RECRUITINGJIS Orthopedics
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RECRUITINGUT Health San Antonio
San Antonio, Texas, United States
RECRUITING...and 2 more locations