Antibiotic Impregnated Bone Graft to Reduce Infection in Hip Replacement.

Last updated: December 4, 2024
Sponsor: University Hospital, Linkoeping
Overall Status: Active - Recruiting

Phase

2/3

Condition

N/A

Treatment

Vancomycin + Tobramycin

Saline

Clinical Study ID

NCT05169229
ABOGRAFT-01
2021-001708-14
  • Ages > 18
  • All Genders

Study Summary

Total hip replacement is the most successful treatment modern healthcare can offer patients to regain quality of life. Periprosthetic joint infection (PJI) is the most common and devastating complication after total hip replacement (THR). Between 0.5 to 2% of primary THR (first time hip replacement), and 8-10% of revision THR (replacement of a hip prosthesis) will become infected.1 The introduction of local antibiotics blended into bone cement has led to a reduction in postoperative infection in primary THR by half.2 Unfortunately, cement can't always be used in relevant quantities.

The number of primary and revision surgeries of the hip is projected to increase dramatically. Therefore, the need for a feasible infection prophylaxis that is applicable for complex primary and revision THR in addition to antibiotics loaded cement is urgent.

Impacted morselized bone allograft is often used in (revision) THR to fill bone defects. Morselized allograft has been used as a carrier for local antibiotic treatment in multiple pilot studies and appears to be an attractive and effective treatment option, both for already infected joints and as a prophylactic measure in high-risk patients (e.g. THR revision surgeries). Nonetheless, a pivotal trial to support its use in THR is lacking. The aim of this pragmatic randomized controlled double blinded drug trial is to investigate whether antibiotic impregnated bone graft (AIBG) decreases the risk of infection after hip arthroplasty compared to controls treated with placebo impregnated bone graft. Patients scheduled for elective THR will be randomized to receive AIBG or a placebo impregnated bone graft. The primary outcome variable will be the number of re-operations due to infections and PJI diagnoses 2 years postoperative.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Age ≥ 18 years

  2. Hip arthroplasty requiring bone graft

  3. Willing to provide informed consent.

  4. For women of childbearing potential; a negative pregnancy test prior to reoperation.

Exclusion

Exclusion Criteria:

  1. Ongoing prosthetic joint infection

  2. Known allergies and contraindications for the use of vancomycin or tobramycin

  3. Mental inability, reluctance, or language difficulties that according toinvestigator judgement, result in difficulty understanding the meaning of studyparticipation

  4. Expected difficulties to complete 2-year follow-up

  5. Women of child bearing potential not using contraception

  6. Pregnant women

  7. Nursing women

Study Design

Total Participants: 850
Treatment Group(s): 2
Primary Treatment: Vancomycin + Tobramycin
Phase: 2/3
Study Start date:
April 01, 2022
Estimated Completion Date:
December 31, 2033

Connect with a study center

  • Universitetssjukhuset Linköping

    Linköping, Region Östergotland 58185
    Sweden

    Active - Recruiting

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