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临床试验/NCT05642013
NCT05642013招募中不适用

SHort Interval Full Two-stage Implant Exchange

University Hospital, Montpellier4 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2023年1月23日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
100
试验地点
4
主要终点
Rate of eligible patients included and benefiting from the standardized protocol without major deviations

研究概览

简要总结

This study is a prospective bicentric feasibility study, which aims to evaluate the feasibility of a two-stage full implant exchange with early prosthesis reimplantation between 16 and 30 days after implants removal for hip or knee prosthetic joint infection.

This study concern 50 patients, prospectively included and compared to the last 50 patients with hip or knee PJI managed with classical two-stage implant exchange.

The duration of the study is 42 months.

详细描述

Prosthetic joint infection (PJI) is a rare but severe complication, with long and complex medico-surgical procedures ang high morbidity. Two-stage full implant exchange is commonly used for PJI, but the best time for prosthesis reimplantation remains unclear. Late reimplantation leads to prolonged immobilization, which can cause decubitus complications and altered joint functionnality.

The hypothesis is that reimplantation between 16 and 30 days after implants removal, earlier than suggested by some relatively old recommandations, associated with 12 weeks antibiotic therapy is a safe and efficient option, allowing shorter immobilization susceptible to improve joint functionnality.

The principal aim of this study is to evaluate the feasibility of a two-stage full implant exchange with early prosthesis reimplantation.

50 patients with knee or hip PJI eligible for two-stage implant exchange will be prospectively included in two french centers.

Surgical procedure will be standardized, with prothesis reimplantation within 16 to 30 days after implants removal, associated with 12 weeks adaptated antibiotherapy according to french recommendations.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Prospective group:
  • Patient over 18 years old
  • Patient managed for a definite osteoarticular infection in a hip or knee prosthesis according to EBJIS definitions (2021) Clinical definition : fistula communicating with the prosthesis, prosthesis exposed / Or biological ≥ 2 samples positive for the same microorganism / And/ or 3000 leukocytes or > 80% of PNN on the synovial fluid / Or histological: visible microorganism, > or = 5 PNN on 5 HPN
  • Patient with an indication for 2-stage surgery:
  • A Impossibility of conservative treatment : infection occurring more than 4 weeks after prosthesis implantation, fistula, documented resistant germ, loosened prosthesis / B Unsuitable 1-stage change: recurrence after 1-stage management, precarious bone capital, documented resistant microorganism, infection without prior microbiological documentation, fistula, surgeon's assessment in disfavor
  • Effective contraception during the research period for fertile women of childbearing age
  • Retrospective group :
  • Patient managed before 31/12/2021 for a definite osteoarticular infection in a hip or knee prosthesis according to EBJIS definitions (2021) Clinical definition : fistula communicating with the prosthesis, prosthesis exposed Or biological ≥ 2 samples positive for the same microorganism And/ or 3000 leukocytes or > 80% of PNN on the synovial fluid Or histological: visible microorganism, > or = 5 PNN on 5 HPN
  • Patient managed by 2 "long" stage surgery with reimplantation time > 6 weeks with an evolutionary follow-up of at least 15 months after the end of antibiotics

排除标准

  • Prospective group :
  • Indication for conservative treatment, 1-stage or 2 long stage surgery
  • Reimplantation by another surgical approach requiring complete skin closure of the initial scar
  • Other surgeries scheduled within 30 days of removal
  • Participation in another interventional treatment study and/or in an exclusion period due to participation in another protocol
  • Subject not affiliated with a social security plan or beneficiary of such a plan
  • Failure to obtain written informed consent
  • Patient with a legal protection measure (guardianship, curatorship)
  • Patient under justice safeguard
  • Pregnant or breastfeeding woman
  • Retrospective group :
  • Refusal to participate
  • Study exit criteria
  • Bacteriological samples positive for fungi
  • Infection not retained after analysis of samples (no sufficient clinical or biological criteria according to EBJIS definition)
  • Withdrawal of consent

结局指标

主要结局

Rate of eligible patients included and benefiting from the standardized protocol without major deviations

时间窗: At 3 months follow-up

Number of eligible patients having been included in the study having benefited from the standardized protocol without major deviations / number of eligible patients according to surgeons or doctors during consultations and hospitalization in orthopedic or infectious disease departments

次要结局

  • Rate of clinical cure(At 15 months follow-up)
  • Rate of re-infection with a different microorganism (superinfection) during follow-up and up to M15(At 15 months follow-up)
  • Articular functionnality(At 15 months follow-up)
  • Quality of life auto-evaluation score(At 15 months follow-up)
  • Antibiotics tolerance(From inclusion to 3 months follow-up)
  • Rate of eligible patients included(At 3 months follow-up)
  • Length of stay(At 15 months follow-up)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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