Actively Recruiting
Evaluation of the Efficiency of the Bone Substitute Cerament-G Locally Delivering Gentamicin in the Treatment of Chronic Osteomyelitis of Long Bones
Led by Hospices Civils de Lyon · Updated on 2024-07-12
220
Participants Needed
15
Research Sites
317 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
Official Title
Evaluation of the Efficiency of the Bone Substitute Cerament-G Locally Delivering Gentamicin in the Treatment of Chronic Osteomyelitis of Long Bones
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient with suspected chronic osteomyelitis (stage III Cierny-Mader) of a long bone (tibia, femur, humerus, forearm) at diaphysis, metaphysis, or epiphysis
- Infection duration more than 3 months
- At least one clinical sign at infected site: spontaneous/supporting pain, fistula or fistula history, serous or purulent flow, bone exposure, local inflammation, or unexplained fever
- At least one radiological sign: bone reshaping with osteolysis or periosteal apposition, intramedullary abscess or fistulous pathway on MRI, or bone sequestration on CT if performed
- Candidate for conventional surgery with corticotomy and endomedullary curettage
- Planned 3 months of systemic antibiotic therapy after surgery
- If osteosynthetic material present, must be removable during surgery
- Possible direct closure or flap within 15 days after surgery
- Male or female aged 18 to 80 years
- Provided written informed consent
- Geographically stable and able to comply with follow-up and treatment
- Affiliated with a social security system
You will not qualify if you...
- Acute hematogenic osteomyelitis (stage I Cierny-Mader)
- Cortical osteitis (stage II Cierny-Mader)
- Septic pseudoarthrosis (stage IV Cierny-Mader)
- Need for skin or soft-tissue flap that cannot be done within 15 days after surgery
- Pregnant, nursing, or planning pregnancy during study
- Participation in another conflicting interventional study
- Known allergy to aminoglycosides (especially gentamicin), sulfites, or calcium hydroxyapatite
- Contraindications to Cerament-G: severe myasthenia (class IV+), severe renal insufficiency, abnormal calcium metabolism
- Endocrine or metabolic disorders affecting bone formation (e.g. Paget's disease, renal osteodystrophy, hyperthyroidism, parathyroid disorder, Ehler-Danlos syndrome, osteogenesis imperfecta)
- Untreated malignant cancers or undergoing radiotherapy/chemotherapy
- Adults under legal protection such as guardianship or trusteeship
AI-Screening
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Trial Site Locations
Total: 15 locations
1
CHU Amiens-Picardie
Amiens, France, 80054
Actively Recruiting
2
CHU de Besançon
Besançon, France, 25030
Not Yet Recruiting
3
CHU Bordeaux
Bordeaux, France, 33076
Actively Recruiting
4
APHP
Boulogne-Billancourt, France, 92104
Not Yet Recruiting
5
CHU Brest
Brest, France, 29200
Actively Recruiting
6
CHU de Caen
Caen, France, 14033
Actively Recruiting
7
CHU de Lille
Lille, France, 59037
Not Yet Recruiting
8
Hospices Civils de Lyon
Lyon, France, 69004
Actively Recruiting
9
Hospices Civils de Lyon
Lyon, France, 69437
Not Yet Recruiting
10
CHRU Nancy
Nancy, France, 54000
Not Yet Recruiting
11
CHU de Nantes
Nantes, France, 44093
Actively Recruiting
12
CHU de Nîmes
Nîmes, France, 30029
Not Yet Recruiting
13
Hospices Civils de Lyon
Pierre-Bénite, France, 69310
Actively Recruiting
14
CHU de Poitiers
Poitiers, France, 86021
Not Yet Recruiting
15
CHU de Toulouse
Toulouse, France, 31059
Actively Recruiting
Research Team
T
Tristan FERRY
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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