Evaluation of the Efficiency of the Bone Substitute Cerament-G Locally Delivering Gentamicin in the Treatment of Chronic Osteomyelitis of Long Bones

NCT04805164 | Recruiting

• 2 other identifiers: 69HCL20_00652020-A02299-30
• Study Type: interventional
• Target: 220
• Locations: 1 country
• Sites: 15

Brief Summary

Chronic osteomyelitis is a serious osteoarticular infection that most often occurs in the long bones (tibia, femur, humerus), responsible for significant morbidity with risk of fracture and amputation. It is due to the presence of bacteria in the bone marrow, sometimes responsible for an intraosseous abscess. Chronic osteomyelitis can have a hematogenous or more often exogenous origin, after trauma or surgery. The bacteria involved have the ability to modify their metabolism and involve persistence mechanisms (such as biofilm) making them difficult to eradicate. The treatment of chronic osteomyelitis requires surgery, i.e. corticotomy, which means opening of the bone cortex to perform an endomedullary curettage to identify the bacteria, remove any sequestration (bone fragments to which the bacteria adhere as biofilm) and reduce the bacterial inoculum. At the same time, or at a second stage, a skin and soft tissue/muscle flap may be required, especially in patients with long-standing disease with embrittlement and adhesion of the skin and soft tissue to the underlying bone. Post-operatively, the patient receives a probabilistic systemic antibiotic therapy and then a systemic antibiotic therapy targeted on the identified germ, for a period of 3 months. The effectiveness of these antibiotics is based on their ability to penetrate bone tissue. Despite the progress made in both antibiotics and surgical treatments, the probability of failure (recurrence of infection) is around 20%, and has unfortunately remained stable for more than 20 years. Cerament-G (BONESUPPORT AB Laboratory, Sweden), a synthetic bone substitute composed of hydroxyapatite, calcium sulphate, and gentamicin, fills the "dead space" formed during surgery, prevents infection of this blood-filled cavity, and promotes bone regeneration within this space (limiting the risk of fracture in the medium and long term). Cerament-G also delivers locally very high doses of gentamicin (concentration of 17.5 mg/mL in the device) for several weeks. Gentamicine is a broad-spectrum bactericidal antibiotic effective against the vast majority of bacteria involved in osteoarticular infections. It provides effective local antibiotic therapy through wide exposure and prolonged concentrations during several weeks. To date, there is no other bone substitute with antibiotics available in France. Two prospective studies have shown that Cerament-G reduces the number of infectious recurrences (about 5%). This innovation is available in France but at a high price (between 2,500 and 4,000 euros) and is not currently reimbursed. However, the use of this product would make it possible to improve the health and quality of life of patients while avoiding certain consumption of resources.

Conditions

Osteomyelitis Chronic

Keywords

Bone infection; chronic osteomyelitis; bone substitute

Outcome Measures

Primary Outcomes (1)

• Incremental Cost-Utility Ratio (ICUR) between the two treatments strategies for chronic long bone osteomyelitis

  At 24 months (M24)

Secondary Outcomes (12)

• Recurrence of bone infection

  At 24 months (M24)

• Intraoperative and Postoperative complications

  From inclusion to 24 months (M24)

• Repeated surgeries for complication

  From first surgery to 24 months (M24)

• Proportion of patients with amputations

  At 24 months (M24)

• Bone healing and bone remodelling/consolidation

  At 12 months (M12)

Study Arms (2)

Innovative strategy

EXPERIMENTAL

usual medical and surgical care with corticotomy and use of a bone substitute (Cerament-G) delivering gentamicin locally (± skin and soft-tissue/muscle flap) and antibiotic therapy.

Procedure: Corticotomy and use of the bone substitute : Cerament-G device.

Reference strategy

ACTIVE COMPARATOR

Medico-surgical usual care with corticotomy (± skin and soft-tissue/muscle flap), and antibiotic therapy.

Procedure: Corticotomy

Interventions

Corticotomy and use of the bone substitute : Cerament-G device. PROCEDURE

Corticotomy and Cerament-G device

Innovative strategy

Corticotomy PROCEDURE

Corticotomy

Reference strategy

Eligibility Criteria

• Age: 18 Years - 80 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patient with suspected chronic osteomyelitis (stage III of the Cierny-Mader classification) of a long bone of the tibia, femur, humerus or forearm, at the diaphysis, metaphysis or epiphysis, defined as follows:
• Supposed inoculation \> 3 months ;
• At least one of the following clinical signs at the suspected infected site:
• Spontaneous or supporting pain ;
• Presence of fistula; or history of fistula discharge
• Presence of serous or purulent flow;
• Presence of bone exposure;
• Local Inflammation;
• Fever in the absence of any other explanation.
• At least one of the following radiological signs at the suspected infected site:
• Bone reshaping with osteolysis or periosteal apposition;
• Presence of intramedullary abscess (if MRI performed);
• Presence of a fistulous pathway to the intramedullary (if MRI performed);
• Presence of bone sequestration visible on CT scan (if CT scan performed).
• Patient in whom conventional surgical treatment of chronic osteomyelitis is possible, with decortication and corticotomy with endomedullary curettage (to eradicate bone sequestrums, reduce the inoculum, and identify the bacterium(s) involved) and secondary intramedullary residual cavity;

You may not qualify if:

• Acute hematogenic osteomyelitis (Cierny-Mader stage I) ;
• Cortical osteitis (Cierny-Mader stage II);
• Septic pseudoarthrosis (Cierny-Mader stage IV);
• Patient requiring an estimated skin and soft-tissue/muscle flap that cannot be done within 15 days after surgery for the treatment of chronic osteomyelitis;
• Woman who is pregnant, nursing or who is considering becoming pregnant during the study period;
• Patient participating in another interventional study that could interfere with it;
• Patient known to have hypersensitivity to aminoglycosides (especially gentamicin), sulfites (including calcium sulfate) or calcium hydroxyapatite;
• Contraindication to the use of Cerament-G: severe myasthenia (class IV or higher according to the MGFA classification), , severe renal insufficiency (creatinine clearance \<30 mL/min according to the Cockcroft-Gault formula, or GFR \< 30 ml/min/1.73² according to the CKD-EPI or MDRDs equation or, dialysis patient), pre-existing disorders of calcium metabolism (total plasma calcium (or total corrected plasma calcium according to albuminemia) outside normal laboratory values);
• Patient with endocrine or metabolic disorders known to affect osteogenesis (e.g., Paget's disease, renal osteodystrophy, hyperthyroidism, parathyroid disorder, Ehler-Danlos syndrome, osteogenesis imperfecta);
• Patient with one or more untreated malignant cancers (including Marjolin's ulcer), or undergoing radiotherapy or chemotherapy;
• Adult patient protected by law, under guardianship or trusteeship.

Sponsors & Collaborators

• Hospices Civils de Lyon: lead

Study Sites (15)

CHU Amiens-Picardie

Amiens, 80054, France

RECRUITING

CHU de Besançon

Besançon, 25030, France

NOT YET RECRUITING

CHU Bordeaux

Bordeaux, 33076, France

RECRUITING

APHP

Boulogne-Billancourt, 92104, France

NOT YET RECRUITING

CHU Brest

Brest, 29200, France

RECRUITING

CHU de Caen

Caen, 14033, France

RECRUITING

CHU de Lille

Lille, 59037, France

NOT YET RECRUITING

Hospices Civils de Lyon

Lyon, 69004, France

RECRUITING

Hospices Civils de Lyon

Lyon, 69437, France

NOT YET RECRUITING

CHRU Nancy

Nancy, 54000, France

NOT YET RECRUITING

CHU de Nantes

Nantes, 44093, France

RECRUITING

CHU de Nîmes

Nîmes, 30029, France

NOT YET RECRUITING

Hospices Civils de Lyon

Pierre-Bénite, 69310, France

RECRUITING

CHU de Poitiers

Poitiers, 86021, France

NOT YET RECRUITING

CHU de Toulouse

Toulouse, 31059, France

RECRUITING

Central Study Contacts

Tristan FERRY

CONTACT

+33 4 72 07 24 81; tristan.ferry@chu-lyon.fr

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 16, 2021
• First Posted: March 18, 2021
• Study Start: October 14, 2021
• Primary Completion (Estimated): November 14, 2027
• Study Completion (Estimated): November 14, 2027
• Last Updated: July 12, 2024

Record last verified: 2024-07

Locations

FR (15)