Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT04805164

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

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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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