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Alpha-Defensin and Synovial Proteins to Improve Detection of Pediatric Septic Arthritis

Primary Purpose

Joint Infection, Infection of Hip Joint (Disorder), Infection of Shoulder Joint

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Synovial Alpha-defensin assay
Synovial Neutrophil elastase assay
Synovial lactate assay
Synovial C-reactive Protein (CRP)
Synovial Staphylococcus spp antigen panel
Synovial Candida spp antigen panel
Synovial Enterococcus faecalis assay
Synovial bacterial culture by BacT/Alert
Synovial Cell count + differential (CBC)
Synovial Gram Stain
Synovial Leukocyte Esterase Test Strips
Synovial PCR for Kingella kingae
Serum Cell count + differential (CBC)
Serum erythrocyte sedimentation rate (ESR)
Serum C-reactive Protein (CRP)
Serum D-dimer
Serum Procalcitonin
Blood Cultures
Optional blood testing per standard of care (ASO, anti-strep, ANA, anti-DS-DNA, HLA-B27, RF, Lyme and other inflammatory/ rheumatologic markers )
Sponsored by
Hospital for Special Surgery, New York
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Joint Infection focused on measuring synovial biomarkers, alpha-defensin, diagnostics, pediatric

Eligibility Criteria

undefined - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria- Septic Cases and Inflamed, Non-Septic Comparators:

  • Synovial fluid is obtained to assess for infection or inflammatory/rheumatologic disease (all medium and large joints will be included: hip, knee, ankle, shoulder, subtalar, elbow, and wrist joints)
  • Patients with recent antibiotic exposure are eligible to participate but will be analyzed separately

Inclusion Criteria- Normative Controls:

  • Patients undergoing a procedure unrelated to infection (the procedure may be arthroscopy, or an open or percutaneous bony or soft tissue procedure)

Exclusion Criteria- All Participants:

  • Family declines to participate/consent
  • Patients with a major joint trauma (such as a documented ligament tear or fracture) within the past 8 weeks are not eligible to have that joint aspirated, but could have another joint aspirated

Exclusion Criteria- Normative Controls:

  • A history of recent infection (within the past 3 months)
  • Received antibiotics in the past 7 days

Sites / Locations

  • Children's Healthcare of AtlantaRecruiting
  • Hospital for Special SurgeryRecruiting
  • Campbell Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Inflamed/Infected Joint

Normative Control

Arm Description

Patients undergoing joint aspiration/debridement due to suspicion of septic joint or rheumatologic/inflammatory condition

Patient undergoing procedure unrelated to infection/inflammation

Outcomes

Primary Outcome Measures

Sensitivity and specificity of experimental tests
Sensitivity and specificity have been selected as these are standard outcome tests when determining the utility of a diagnostic test.

Secondary Outcome Measures

Full Information

First Posted
May 8, 2018
Last Updated
July 31, 2023
Sponsor
Hospital for Special Surgery, New York
Collaborators
Pediatric Orthopaedic Society of North America, Children's Healthcare of Atlanta, Campbell Clinic, CD Diagnostics
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1. Study Identification

Unique Protocol Identification Number
NCT03704766
Brief Title
Alpha-Defensin and Synovial Proteins to Improve Detection of Pediatric Septic Arthritis
Official Title
Alpha-Defensin and Synovial Proteins to Improve Detection of Pediatric Septic Arthritis
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 28, 2016 (Actual)
Primary Completion Date
May 2024 (Anticipated)
Study Completion Date
May 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital for Special Surgery, New York
Collaborators
Pediatric Orthopaedic Society of North America, Children's Healthcare of Atlanta, Campbell Clinic, CD Diagnostics

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Differentiating between septic arthritis and other causes of joint inflammation in pediatric patients is challenging and of the utmost importance because septic arthritis requires surgical debridement as part of the treatment regimen. The current gold standard to diagnose septic arthritis in children is a positive synovial fluid culture; however, joint cultures may take several days to return. If a bacterial infection is present, it requires immediate surgical intervention in order to prevent lasting articular cartilage damage. Frequently surgeons must decide whether to surgically debride a joint before culture results are available. There is no single lab test or clinical feature that reliably indicates bacterial infection over other causes of joint inflammation. The alpha-defensin assay has shown high sensitivity and specificity for joint infection in other studies.The purpose of this study is to determine the sensitivity and specificity of several synovial biomarkers for diagnosing pediatric septic arthritis.
Detailed Description
The purpose of this study is to determine if alpha-defensin and other proteins present in joint fluid may be able to rapidly diagnose bacterial joint infections. Patients with suspected joint infection typically undergo joint aspiration so that tests can be performed to help diagnose joint infection, including gram stain, cell count, and culture. Patients under 18 years old that are undergoing sampling of their joint fluid due to suspicion of infection or inflammation will be enrolled in this multi-center trial. Joint fluid will also be sampled from normative controls made up of patients who are undergoing an unrelated procedure without inflammation or infection. Joint fluid from patients with suspected inflammation/infection and from normative controls will be analysed for presence of alpha-defensin, leukocyte esterase, neutrophil elastase, synovial C-reactive protein, and synovial lactate. The alpha-defensin assay has shown high sensitivity and specificity for joint infection in other studies. Additionally a Staphylococcus spp antigen panel, Candida spp antigen panel, Enterococcus faecalis assay, BACTAlert culture, cell count plus differential, gram stain, and aerobic, anaerobic, and fungal cultures will be done using synovial fluid. A synovial fluid PCR for Kingella kingae will be performed if the patient is under eight years of age. Blood tests will include cell count and differential, erythrocyte sedimentation rate, C-reactive protein, procalcitonin, and D-dimer, as well as relevant inflammatory or rheumatologic marker tests. Results from these tests will be compared to joint fluid culture which the gold standard for diagnosing bacterial infection. The study includes 1 visit per patient, the standard of care visit in which the patient would be undergoing joint aspiration or arthroscopy. Once data has been collected, the sensitivity and specificity will be determined for these experimental tests both individually and in combination.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Joint Infection, Infection of Hip Joint (Disorder), Infection of Shoulder Joint, Septic Arthritis
Keywords
synovial biomarkers, alpha-defensin, diagnostics, pediatric

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants are assigned as either cases of infection/inflammation, or normative controls, and receive the same diagnostic testing for the duration of the study.
Masking
ParticipantCare Provider
Masking Description
For patients with inflamed joints, the medical team will be blind to the results of the alpha-defensin assay and other experimental tests for a period of 2 weeks, after which results may be divulged to the clinical team at their request. As such, the results will not influence the physician/surgeons' decision for acute treatment of the patient, as the decision to treat suspected septic arthritis is typically made within 24 hours, and the final diagnosis is made within 2 weeks (pending culture results). As the testing of the leukocyte esterase strips will occur in the operating room, the surgeon will not be blinded to these results. A blinded team member will read the pictures of all of the leukocyte test strip results at once, after they have all been collected. The patient will be made aware of results at the physician/surgeon's discretion. For normative controls, the results of experimental testing will not be divulged to the clinical team or to the patient.
Allocation
Non-Randomized
Enrollment
442 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Inflamed/Infected Joint
Arm Type
Experimental
Arm Description
Patients undergoing joint aspiration/debridement due to suspicion of septic joint or rheumatologic/inflammatory condition
Arm Title
Normative Control
Arm Type
Active Comparator
Arm Description
Patient undergoing procedure unrelated to infection/inflammation
Intervention Type
Diagnostic Test
Intervention Name(s)
Synovial Alpha-defensin assay
Intervention Description
One of the synovial fluid (joint fluid) tests that will be performed by the outside lab, CD Diagnostics.
Intervention Type
Diagnostic Test
Intervention Name(s)
Synovial Neutrophil elastase assay
Intervention Description
One of the synovial fluid (joint fluid) tests that will be performed by the outside lab, CD Diagnostics.
Intervention Type
Diagnostic Test
Intervention Name(s)
Synovial lactate assay
Intervention Description
Synovial Fluid (joint fluid) will be sent out to CD Diagnostics for this test.
Intervention Type
Diagnostic Test
Intervention Name(s)
Synovial C-reactive Protein (CRP)
Intervention Description
One of the synovial fluid (joint fluid) tests that will be performed by the outside lab, CD Diagnostics.
Intervention Type
Diagnostic Test
Intervention Name(s)
Synovial Staphylococcus spp antigen panel
Intervention Description
One of the synovial fluid (joint fluid) tests that will be performed by the outside lab, CD Diagnostics.
Intervention Type
Diagnostic Test
Intervention Name(s)
Synovial Candida spp antigen panel
Intervention Description
One of the synovial fluid (joint fluid) tests that will be performed by the outside lab, CD Diagnostics.
Intervention Type
Diagnostic Test
Intervention Name(s)
Synovial Enterococcus faecalis assay
Intervention Description
One of the synovial fluid (joint fluid) tests that will be performed by the outside lab, CD Diagnostics.
Intervention Type
Diagnostic Test
Intervention Name(s)
Synovial bacterial culture by BacT/Alert
Intervention Description
The synovial fluid (joint fluid) sent to CD Diagnostics for testing will also be cultured to see if any organisms grow.
Intervention Type
Diagnostic Test
Intervention Name(s)
Synovial Cell count + differential (CBC)
Intervention Description
One of the synovial fluid (joint fluid) tests that will be performed by the outside lab, CD Diagnostics.
Intervention Type
Diagnostic Test
Intervention Name(s)
Synovial Gram Stain
Intervention Description
This will be performed by CD Diagnostics if any organisms are present in the synovial fluid.
Intervention Type
Diagnostic Test
Intervention Name(s)
Synovial Leukocyte Esterase Test Strips
Intervention Description
These test strips will be tested at the hospital where the patient is being seen, a few drops of synovial fluid will be used on the strip.
Intervention Type
Diagnostic Test
Intervention Name(s)
Synovial PCR for Kingella kingae
Intervention Description
In participants < 8 years old, a sample of synovial fluid will be tested for Kingella kingae using PCR.
Intervention Type
Diagnostic Test
Intervention Name(s)
Serum Cell count + differential (CBC)
Intervention Description
A blood test performed at the hospital.
Intervention Type
Diagnostic Test
Intervention Name(s)
Serum erythrocyte sedimentation rate (ESR)
Intervention Description
A blood test performed at the hospital.
Intervention Type
Diagnostic Test
Intervention Name(s)
Serum C-reactive Protein (CRP)
Intervention Description
A blood test performed at the hospital.
Intervention Type
Diagnostic Test
Intervention Name(s)
Serum D-dimer
Intervention Description
A blood test performed at the hospital.
Intervention Type
Diagnostic Test
Intervention Name(s)
Serum Procalcitonin
Intervention Description
A blood test performed at the hospital.
Intervention Type
Diagnostic Test
Intervention Name(s)
Blood Cultures
Intervention Description
Blood will be cultured at the hospital to see if any organisms grow.
Intervention Type
Diagnostic Test
Intervention Name(s)
Optional blood testing per standard of care (ASO, anti-strep, ANA, anti-DS-DNA, HLA-B27, RF, Lyme and other inflammatory/ rheumatologic markers )
Intervention Description
In patients with suspected inflammation/infection, there are other blood tests which may be standard of care and used for diagnosis.
Primary Outcome Measure Information:
Title
Sensitivity and specificity of experimental tests
Description
Sensitivity and specificity have been selected as these are standard outcome tests when determining the utility of a diagnostic test.
Time Frame
Interim analysis at 2 years of study recruitment

10. Eligibility

Sex
All
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria- Septic Cases and Inflamed, Non-Septic Comparators: Synovial fluid is obtained to assess for infection or inflammatory/rheumatologic disease (all medium and large joints will be included: hip, knee, ankle, shoulder, subtalar, elbow, and wrist joints) Patients with recent antibiotic exposure are eligible to participate but will be analyzed separately Inclusion Criteria- Normative Controls: Patients undergoing a procedure unrelated to infection (the procedure may be arthroscopy, or an open or percutaneous bony or soft tissue procedure) Exclusion Criteria- All Participants: Family declines to participate/consent Patients with a major joint trauma (such as a documented ligament tear or fracture) within the past 8 weeks are not eligible to have that joint aspirated, but could have another joint aspirated Exclusion Criteria- Normative Controls: A history of recent infection (within the past 3 months) Received antibiotics in the past 7 days
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Grace Wang, BA
Phone
212-774-2121
Email
wangg@hss.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emily R Dodwell, MD, MPH
Organizational Affiliation
The Hospital for Special Surgery
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Healthcare of Atlanta
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30342
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jack Goldberg, MS
Phone
678-686-6864
Email
Jack.Goldberg@choa.org
First Name & Middle Initial & Last Name & Degree
Tim Schrader, MD
Phone
(404) 255-1933
Facility Name
Hospital for Special Surgery
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Grace Wang, BA
Phone
212-774-2121
Email
wangg@hss.edu
First Name & Middle Initial & Last Name & Degree
Emily R Dodwell, MD, MPH
Phone
212-606-1451
First Name & Middle Initial & Last Name & Degree
Emily R Dodwell, MD, MPH
First Name & Middle Initial & Last Name & Degree
Joseph J Ruzbarsky, MD
First Name & Middle Initial & Last Name & Degree
Roger F Widmann, MD
First Name & Middle Initial & Last Name & Degree
Daniel W Green, MD
First Name & Middle Initial & Last Name & Degree
John S Blanco, MD
First Name & Middle Initial & Last Name & Degree
David M Scher, MD
First Name & Middle Initial & Last Name & Degree
Shevaun M Doyle, MD
First Name & Middle Initial & Last Name & Degree
Peter D Fabricant, MD, MPH
First Name & Middle Initial & Last Name & Degree
Christine M Salvatore, MD
First Name & Middle Initial & Last Name & Degree
Matthew Greenblatt, MD, PhD
First Name & Middle Initial & Last Name & Degree
Huong Do, MS
Facility Name
Campbell Clinic
City
Collierville
State/Province
Tennessee
ZIP/Postal Code
38017
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jonathan Rowland
Phone
901-287-5413
Email
Jonathan.Rowland@lebonheur.org
First Name & Middle Initial & Last Name & Degree
Derek Kelly, MD
Phone
(901) 759-3100

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Collaborating sites will share de-identified patient data with the primary site, the Hospital for Special Surgery. The Hospital for Special Surgery, will incorporate de-identified aggregated data into a separate de-identified aggregated data sat to be provided to all study sites, but individual participant data will not be shared with all sites.
Citations:
PubMed Identifier
25256621
Citation
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Links:
URL
https://pubmed.ncbi.nlm.nih.gov/22608686/
Description
Leukocyte esterase reagent strips for the rapid diagnosis of periprosthetic joint infection

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Alpha-Defensin and Synovial Proteins to Improve Detection of Pediatric Septic Arthritis

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