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Rifabutin Versus Rifampicin for Treatment of Staphylococcal PJI Treated With DAIR (RIFAMAB)

T

Tourcoing Hospital

Status and phase

Enrolling
Phase 3

Conditions

Prosthetic Infection

Treatments

Drug: Rifabutin
Drug: Rifampicin

Study type

Interventional

Funder types

Other

Identifiers

NCT04672525
RIPH_2019_01

Details and patient eligibility

About

Rifampicin, is key in the treatment of staphylococcal PJIs. Rifabutin has a better profile of tolerance than rifampicin regarding the risk of interaction with concomitant medications and liver disorders. The hypothesis is that rifabutin may be an alternative antibiotic option as efficient as rifampicin for the treatment of staphylococcal PJIs, with a better safety profile. The investigator aim to demonstrate the non-inferiority of rifabutin as compared with rifampicin prescribed in combination treatment for PJIs.

Enrollment

436 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Hip or knee Prosthetic joint infection treated by debridement, antibiotic therapy initiation and retention of prothesis (DAIR strategy)

  2. Infected with at least one of the following microorganisms:

    1. Staphylococcus aureus
    2. Coagulase-negative staphylococci
  3. Microorganisms susceptible to rifampicin and at least one other antibiotic suitable for the treatment of PJI (e.g., penicillin, fluoroquinolone, (doxy/mino)cycline, oxazolidinone, cotrimoxazole, daptomycin, glycopeptide, macrolide, fusidic acid), regardless of sensitivity to methicillin.

  4. Age ≥ 18 years

  5. At least 2 days of appropriate (i.e., covering pathogen(s) identified in the intraoperative samples) empirical agents are needed. Pre-randomization antimicrobial therapy could be: flucloxacillin, oxacillin, vancomycin, daptomycin. β-lactam plus β-lactamase-inhibitors (e.g. ampicillin+sulbactam, piperacillin+tazobactam), cephalosporins (except ceftazidime), carbapenems, teicoplanin, ceftaroline, ceftobiprole.

  6. Signed Inform consent

  7. Patient having the rights to French social insurance

  8. For women of childbearing potential i.e. fertile, following menarche and until becoming post-menopausal unless permanently sterile and excluding oestroprogestative-based contraception, any effective contraceptive: vasectomy (for men), intrauterine device copper, feminine sterilization, condom, sexual abstinence is required. A postmenopausal state is defined as no menses for 12 months without an alternative medical cause

Exclusion criteria

  1. Suspicion of reduce absorption of oral treatment due to abdominal disorder Known or suspected malabsorption (imperfect absorption of food material by the small intestine)
  2. Polymicrobial infection due to other than staphylococcus species susceptible to rifampicin
  3. Known or suspected allergy to rifabutin and/or rifampicin
  4. Diagnosis of endocarditis associated to PJI
  5. Renal transplant or Chronic kidney disease with an eGFR of less than 30ml/min/1.73m²
  6. Other Solid Organ Transplant
  7. Liver cirrhosis, Child-Pugh score C
  8. Any other concomitant infection which required a prolonged course of intravenous antibiotic therapy
  9. Oestroprogestative-based contraception
  10. Oral anticoagulant drugs
  11. Other drug-drug interaction that contraindicated rifampicin or rifabutin
  12. Porphyria
  13. Unable to take oral treatment
  14. Receive empirical postoperative antibiotic treatment by rifampicin or rifabutin prior to randomization
  15. Pregnancy or lactating women
  16. Curator or guardianship or patient placed under judicial protection
  17. Participation in other interventional research during the study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

436 participants in 2 patient groups

RIFAMPICIN
Active Comparator group
Description:
Patient with staphylococcal PJI, treated with DAIR strategy, and randomized in the control group will receive rifampicin in association with another antibiotic except rifabutin, as-per recommendations for 12 weeks.
Treatment:
Drug: Rifampicin
RIFABUTIN
Experimental group
Description:
Patient with staphylococcal PJI treated with DAIR strategy, and randomized in the experimental group, will receive rifabutin in association with another antibiotic except rifampicin, as-per recommendations for 12 weeks.
Treatment:
Drug: Rifabutin

Trial contacts and locations

30

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Central trial contact

Solange TREHOUX; Eric SENNEVILLE, MD PhD

Data sourced from clinicaltrials.gov

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