Efficacy and Safety of Intravenous Fosfomycin in Prosthetic Joint Infection

Prosthetic Joint Infection Clinical Trial

Official title:

Efficacy and Safety of Intravenous Fosfomycin in Prosthetic Joint Infection (PJI) Caused by Staphylococci, Streptococci, Enterococci and Gram-negative Bacilli, Including Mixed Infections and Culture Negative PJI's ("PROOF-Study")

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05211011
• Other study ID #: PROOF
• Status: Active, not recruiting
• Phase: Phase 4
• Start date: January 23, 2018
• Est. completion date: April 30, 2023

Study information

• Verified date: January 2022
• Source: Charite University, Berlin, Germany
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The PROOF Study is an open prospective interventional non-randomized study which aim is to determine the outcome / effect and safety of fosfomycin in patients with hip, knee or shoulder PJI.

Description:

To confirm a non-inferior effect and the safety of the investigated antimicrobial fosfomycin regimen in PJI of the hip, knee or shoulder against an assumed 80% effect (PJI-free proportion within one year for standard antibiotics aside fosfomycin), following a standardized surgical therapy involving retention, one-stage exchange or two-stage exchange (with short or long interval).

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 226
• Est. completion date: April 30, 2023
• Est. primary completion date: April 30, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Informed consent has been obtained (prior to planned surgical PJI treatment);

2. Subject is =18 years of age;

3. Subject has either a culture negative or a culture positive PJI of the hip, knee or shoulder prosthesis: (i) visible purulence of a preoperative aspirate or intraoperative periprosthetic tissue (as determined by the surgeon),or (ii) presence of a sinus tract communicating with the prosthesis, or (iii) acute inflammation in intraoperative permanent tissue sections by histopathology (as determined by the pathologist), or (iv) microbial growth in preoperative joint aspirate, intraoperative periprosthetic tissue or sonication fluid of the removed implant (>50 CFU/ml sonication fluid), or (v) synovial fluid with >2000 leukocytes/µl or >70% granulocytes; or reasonable evidence for a suspected PJI (based on clinical, laboratory, and radiological criteria) to undergo joint surgery to proof the PJI diagnosis (according to standard of care, Zimmerli W et al. NEJM 2004);

4. For culture positive PJI's at least one of the following isolates:

staphylococci (fosfomycin MHK = 32 mg/ml), streptococci (MHK = 128 mg/ml), enterococci (MHK = 128 mg/ml), fosfomycin susceptible gram-negative bacilli, including also mixed infections with other pathogens (fosfomycin susceptible or not);

5. Subject is planned to/will undergo appropriate surgical procedure following the state of the art PJI treatment algorithm, which includes either debridement & retention of the prosthesis or exchange of the prosthesis. The exchange includes a one-stage exchange, two-stage prosthesis exchange with a short interval (2- 3 weeks) or long interval (6-8 weeks), according to the treatment algorithm;

6. Subject is willing to participate in the study, follow protocol study treatment regimen, and comply with all planned follow-up assessments.

Exclusion Criteria:

1. Allergy or intolerance (or other contraindication) to fosfomycin;

2. Isolation of fungi (molds or yeasts) or mycobacteria;

3. Isolation of one of the following pathogens: staphylococci fosfomycin MHK > 32 mg/ml, streptococci MHK > 128 mg/ml, enterococci MHK > 128 mg/ml , fosfomycin resistant gramnegative bacilli;

4. Severely compromised bone/soft tissue pre or during surgery (if during surgery:

exclusion/withdrawalbefore IMP application);

5. Pregnancy, and/or woman wishing to become pregnant;

6. Breast-feeding;

7. Women of childbearing potential without at least one of the following contraception methods: correctly placed coopercontaining or progestin-containing intrauterine device (IUD); female condom used WITH a spermicide (i.e. foam gel, film, cream, or suppository); bilateral tubal ligation/bilateral salpingectomy or bilateral tubal occlusive procedure (at least till the end of the ambulatory treatment phase);

8. Subject has been previously enrolled in this study or was enrolled in another interventional medicinal product or medical device study in the last 30 days;

9. Subject had prior exposure to fosfomycin within the past 4 weeks;

10. Inability to read and understand the participant's information;

11. Subjects institutionalized by warrant or court order;

12. Employees of the sponsor or an involved CRO;

13. In pre surgery culture negative patients: All isolates unsusceptible to fosfomycin after surgery (exclusion / early withdrawal after surgery);

14. Suspected PJI not proven after surgery (exclusion / early withdrawal after surgery).

Related Conditions & MeSH terms

• Arthritis, Infectious
• Communicable Diseases
• Infections
• Prosthetic Joint Infection

Intervention

Drug:
• Fosfomycin
Infectofos 5 g

Locations

Country	Name	City	State
Germany	Charité	Berlin
Germany	BG Universitätsklinikum Bergmannsheil	Bochum	Nordrhein-Westfalen
Germany	Universitätsklinikum Bonn	Bonn
Germany	Städtisches Klinikum Dresden	Dresden
Germany	Universitätsklinikum Dresden	Dresden
Germany	Universitätsklinikum Düsseldorf	Düsseldorf
Germany	Waldkrankenhaus Rudolf Elle GmbH	Eisenberg
Germany	St. Josef Krankenhaus Essen-Werden	Essen
Germany	Helios Klinikum Hildesheim	Hildesheim
Germany	Krankenhaus Köln-Merheim	Köln
Germany	Universitätsmedizin Mainz	Mainz
Germany	St. Franziskus Hospital Münster	Münster
Germany	Universitätsklinikum Regensburg	Regensburg
Germany	Sophien- und Hufelandklinikum GmbH Weimar	Weimar
Germany	Krankenhaus Johanneum	Wildeshausen
Germany	Krankenhaus St. Josef	Wuppertal

Sponsors (2)

Lead Sponsor	Collaborator
Charite University, Berlin, Germany	Pro-Implant Foundation

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Infection cure rate	Proportion of patients free of PJI relapse (i.e. infection cure rate) within 1 year after inclusion. Relapse is defined as new PJI diagnosis more than 4 weeks after the last surgical intervention of the initial 12 week treatment period.	1 year
Secondary	Infection cure rate	Proportion of patients free of Prosthetic Joint-Infection relapse (infection cure rate) within 2 years after inclusion	2 years
Secondary	Proportion of patients with revision	Proportion of patients with revision (surgical intervention with or without prosthesis removal >4 weeks after last surgical intervention of the initial 12 week treatment period)	1 year
Secondary	Proportion of patients with revision due to hematogenous versus non-hematogenous infection	Proportion of patients with revision due to hematogenous (acute onset with duration of symptoms <3 weeks and onset of symptoms is >3 months after last surgery) versus non-hematogenous infection	1 year
Secondary	Proportion of patients with unscheduled early revisions	Proportion of patients with unscheduled early revisions (<4 weeks after last scheduled surgical intervention - deep (= bone/joint) revision versus superficial (= skin-soft tissue) revision)	1 year
Secondary	Proportion of patients with aseptic revision	Proportion of patients with aseptic revision	1 year
Secondary	Proportion of patients with implant failure	Proportion of patients with implant failure (any functionally affected or pain producing implant, clinically relevant abnormal laboratory test result indicating PJI, or presence of radiological signs of loosening, according to the investigator (Yes/No))	1 year
Secondary	Proportion of patients with treatment failure	Proportion of patients with treatment failure (insufficient primary therapy or PJI relapse)	1 year
Secondary	Proportion of patients with initially sufficient versus insufficient primary therapy	Proportion of patients with initially sufficient versus insufficient primary therapy (defined by the judgement of the investigator, based on combined clinical, laboratory, microbiological and radiological criteria, e.g. clear reduction of wound secretion)	1 year
Secondary	Specific functional joint scores	Development and changes vs baseline of specific functional joint scores	1 year
Secondary	EQ5D5L	EQ5D5L (in particular for 1 year follow up)	1 year
Secondary	Safety and tolerability of fosfomycin	Safety and tolerability of fosfomycin will be evaluated by measuring the frequency of adverse events, including potential side effects	1 year
Secondary	Peak Plasma Concentration (Cmax)	Pharmacokinetic profile of fosfomycin in plasma	1 year