Skip to main content
OpenTrials
Recruiting

NCT Number: NCT05642013

SHort Interval Full Two-stage Implant Exchange

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.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU de Montpellier - Hôpital Saint-Eloi, Montpellier, France

Loading trial locations.

About this study

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.

Patients will be compared to the last 50 patients with hip or knee PJI managed with classical two-stage implant exchange in these centers until december 2021 (retrospective group).

Follow up consists of 7 clinical evaluations, from inclusion until month15 after prosthesis removal.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

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

Treatment and study plan

Early prosthesis reimplantation

Procedure

Early prosthesis reimplantation, within 16 to 30 days after implants removal

Retrospective analysis of medical records

Other

Analysis of 50 records of operated patients managed with classical two-stage implant exchange

Primary outcomes

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

    Time frame: 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

Secondary outcomes

  1. Rate of eligible patients included

    Time frame: At 3 months follow-up

    Number of eligible patients included in the study / number of eligible patients according to surgeons or doctors during consultations and hospitalization in orthopedic or infectious disease departments

  2. Rate of clinical cure

    Time frame: At 15 months follow-up

    Number of patients included without signs of infectious relapse to the same germ or persistence of the initial infection at M15 / number of patients included who benefited from the standardized protocol without major deviations., compared to clinical cure rate in retrospective group

  3. Rate of re-infection with a different microorganism (superinfection) during follow-up and up to M15

    Time frame: At 15 months follow-up

    Number of patients who presented a reinfection according to the EBJIS criteria with a germ different from the initial organism(s) during follow-up / number of patients included who benefited from the standardized protocol without major deviations, compared to reinfection rate in retrospective group

  4. Length of stay

    Time frame: At 15 months follow-up

    Cumulative length of stay in hospital (medicine or surgery wards) or in follow-up care compared to cumulative length of stay in retrospective group

  5. Articular functionnality

    Time frame: At 6 months follow-up

    Knee Society Score or Harris Hip Score

  6. Articular functionnality

    Time frame: At 15 months follow-up

    Knee Society Score or Harris Hip Score

  7. Quality of life auto-evaluation score

    Time frame: At inclusion

    EQ-5D-5L score (auto-questionnary)

  8. Quality of life auto-evaluation score

    Time frame: At 3 months follow-up

    EQ-5D-5L score (auto-questionnary)

  9. Quality of life auto-evaluation score

    Time frame: At 15 months follow-up

    EQ-5D-5L score (auto-questionnary)

  10. Antibiotics tolerance

    Time frame: From inclusion to 3 months follow-up

    Evaluation of antibiotics tolerance by clinical +/- biological evaluation

Study contacts

Contact information is provided by the study sponsor or research team.

Nathalie PANSU, MD

CONTACT

[email protected]

+33467339510

Vincent LE MOING, MD PhD

CONTACT

[email protected]

+33467339510

Sponsors and collaborators

Lead sponsor

University Hospital, Montpellier

Other

Registry information

Acronym: SHIFT

Important dates

Study start
2023
Primary completion
2026
Study completion
2027
First posted
Dec 8, 2022
Registry last updated
Aug 6, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.