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Prosthetic Joint InfectionNCT03694925

Diagnostic Utility of a Novel Point-of-Care Test of Calprotectin for Revision Total Knee Arthroplasty

An observational study of Prosthetic Joint Infection, run by The Cleveland Clinic at 2 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to investigate whether there are quantifiable differences in the level of calprotectin in the synovial fluid that allow separation of different modes of joint implant failure (e.g. infected, aseptic loosening). Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Prosthetic Joint Infection
What is being tested?
Calprotectin test
How many people
156 participants
Where
2 sitesUnited States
Study dates
29 Oct 2018to 4 Mar 2020
Phase
Observational
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Three groups: Primary total knee arthroplasty Aseptic revision total knee arthroplasty Septic revision total knee arthroplasty

Who may be able to join

  • Subject is ≥18 years of age
  • Patient with a diagnosis of OA (for primary TKA only)
  • Subject has had no recent injections or surgeries of the joint (within past 6 weeks)
  • Subject has or will have all of the medical tests required to allow MSIS classification
  • Subject signs informed consent form

Who cannot join

  • Subjects with a diagnostic synovial fluid specimen collection within the past 7 days
  • Results are not available for medical tests required to perform MSIS classification
  • Sample was obtained via lavage
  • Quantity not sufficient (at least 1 ml required)

Trial locations and contacts

2 sites in 1 country.

United States2 sites
  • Cleveland Clinic

    Cleveland, Ohio, 44195

  • Cleveland Clinic Florida

    Weston, Florida, 33331

Other trials in United States

About this study

Official title: Diagnostic Utility of a Novel Point-of-Care Test of Calprotectin for Revision Total

The purpose of this study is to investigate whether there are quantifiable differences in the level of calprotectin in the synovial fluid that allow separation of different modes of joint implant failure (e.g. infected, aseptic loosening). A subset of primary TKA patients (with history of OA) will be included as a baseline.

Read the detailed description

Calprotectin is a biomarker closely associated with leucocytes in general, and is present in high volumes in neutrophil cells. Calprotectin is also produced by infiltrating monocytes and macrophages, where calprotectin is released upon phagocytosis. In neutrophils, calprotectin is stored intracellularly and are released upon activation of the cell. The determination of number of neutrophils and proportion of neutrophils out of total number of inflammatory cells is a diagnostic strategy commonly used in diagnosis of infection. Upon encounter with a pathogen, neutrophils have several strategies to fight infections , and produce high-levels of calprotectin. Activation of neutrophils, and release of calprotectin, can be for any reason causing activation of the complement system and aseptic Inflammatory responses. Moreover, Calprotectin is a danger associated molecular patterns (DAMP) signal influencing the inflammatory responses. The level of activated neutrophils in PJI provide basis of the presence of calprotectin in the synovial fluid of PJI patients, and thus, for calprotectin as a potential biomarker for PJI. Calprotectin-levels in the synovial fluid do not merely reflect the level of leucocytes and neutrophils present in the synovial fluid, but levels are correlated to the WBC content. Calprotectin is likely to reflect the number of activated cells and surpass the diagnostic accuracy of total WBC counts and neutrophil percentage for PJI diagnosis.

A level of calprotectin of 50 mg/L in the synovial fluid has very good diagnostic accuracy for PJI, supported by area under the curve values of more than 0.9. In a subgroup analysis for patients with chronic PJI, a NPV of 97% was observed. The excellent NPV may assist in the orthopaedic clinic to rule out the presence of infection and consider diagnostic alternatives for aseptic loosening and pain revision of the joint patient. A rapid and accurate distinction between these two causes is important as PJI and aseptic loosening are managed differently with regards to surgical Intervention and followup.

Point of Care Test diagnostics by lateral flow devices provides reliable test results within minutes of sample collection. Currently, Calprotectin can be detected by such lateral flow devices (developed by Orthogenics, Tromsø, Norway). The speed and ease of use of this test allows for diagnosis at patient's bed side. These tests can be applied in the physician's office, operating room, an ambulance, the home, the field, or in the hospital. As the results are timely they allow rapid diagnostic and identifies treatment alternatives for the patient. This technology empowers clinicians to make decisions at the "point-of-care" and can have significant impact on health care delivery and ability to address challenges of health disparities. However, it is important to validate the diagnostic utility of calprotectin POC in a diverse set of patients undergoing revision arthroplasty.

Being tested
Calprotectin test

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Calprotectin testDiagnostic test

    Calprotectin will be measured both by ELISA and point of care test.

Study groups in NCT03694925
Study groupRoleWhat they receive
Primary total knee arthroplastyPrimary TKA patients included in the study, to provide a baseline level for calprotectin.
Receives: Diagnostic Test: Calprotectin test
Aseptic revision total knee arthroplastyAseptic revision TKA patients included in the study. These are patients who are not considered infected according to Musculoskeletal Infection Society criteria for infection.
Receives: Diagnostic Test: Calprotectin test
Revision septic total knee arthroplastySeptic revision TKA patients included in the study. These are patients who are considered infected according to Musculoskeletal Infection Society criteria for infection.
Receives: Diagnostic Test: Calprotectin test

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Calprotectin POC

    lateral flow point of care test

    Measured: Day of surgery

Secondary outcomes (1)
  1. Calprotectin ELISA

    ELISA analysis

    Measured: Day of surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Oct 2018
  2. Study start29 Oct 2018
  3. Primary completion7 Jan 2020
  4. Study completion4 Mar 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Prospective
Enrolment
156 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03694925
Sponsor's protocol ID
18-882
Status last verified
Nov 2020
First submitted
2 Oct 2018
Last updated
17 Dec 2020
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: The only group we will be sharing data with is the company (Lyfstone) which is funding the research.

Questions about this trial

What is this clinical trial studying?

An observational study of Prosthetic Joint Infection, run by The Cleveland Clinic at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 17 Dec 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 17 Dec 2020). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Calprotectin POC (time frame: Day of surgery). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Dec 2020.

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