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Percutaneous Punch Biopsy for Diagnosis of Septic and Aseptic Prosthetic Joint Failure (SHARP)

Primary Purpose

Wear of Articular Bearing Surface of Internal Prosthetic Joint, Infection Prosthetic, Infections Joint Prosthetic

Status
Unknown status
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Punch biopsy
Sponsored by
Vivantes Netzwerk für Gesundheit GmbH
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Wear of Articular Bearing Surface of Internal Prosthetic Joint focused on measuring prosthetic joint, infection, wear particles, prosthetic failure, antibiotics, biopsy, joint tap

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Preceding implantation of a shoulder, hip or knee endoprosthesis
  • Acute or chronic pain in the joint
  • Periprosthetic fracture
  • Instability of the endoprosthesis
  • Indications of wear / insufficiency of the enclosed plastic spacers
  • Indications of metal abrasion
  • Primary misalignment of the implant

Exclusion Criteria:

  • Confirmed periprosthetic infection
  • Proven allergy to fast-acting local anesthetics

Sites / Locations

  • Vivantes Humboldt-KrankenhausRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Joint tap

Punch biopsy

Arm Description

Joint tap and aspiration of synovial fluid

Punch biopsy of a prosthetic joint and extraction of 5-7 biopsies from the synovial membrane

Outcomes

Primary Outcome Measures

Improved diagnostic accuracy
Comparison of the specificity and sensibility of microbiological results for punch biopsies, the synovial fluid tap, pre-interventional blood Analysis, arthroscopic biopsies for confirmation/exclusion of a bacterial or fungal periprosthetic infection

Secondary Outcome Measures

Rate of chronic periprosthetic low-grade-infections
The incidence of hidden chronic periprosthetic infections
Correlation of microbiological results from percutaneous Punch biopsy with intraoperative findings at Revision
Correlation of pre-revision microbiological findings and the samples taken during the endoprosthesis replacement operation, in particular the sonicate of the prosthesis and the periprosthetic membrane (gold standard for infection diagnostics)
Total Cost of Infection Diagnostics for various used methods
Comparison of the respective Overall Costs for diagnostics of acute and chronic periprosthetic infections using a joint-tap, the novel punch biopsy method and arthroscopic biopsy
Rate of prosthetic failure due to wear particles
Incidence of presence of wear particles in pathomorphological examinations of the punch biopsies and the samples taken during the replacement operation
Correlation of Synovialitis score and microbiological findings
Correlation of Synovialitis score in pathomorphological examinations and microbiological verification of an acute or chronic periprosthetic infection

Full Information

First Posted
August 25, 2020
Last Updated
November 2, 2020
Sponsor
Vivantes Netzwerk für Gesundheit GmbH
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1. Study Identification

Unique Protocol Identification Number
NCT04620395
Brief Title
Percutaneous Punch Biopsy for Diagnosis of Septic and Aseptic Prosthetic Joint Failure
Acronym
SHARP
Official Title
Clinical Investigation of Septic and Aseptic Prosthetic Joint Failure - Percutaneous Punch Biopsy as a Novel Way of Diagnosis Confirmation
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
August 20, 2020 (Actual)
Primary Completion Date
January 31, 2022 (Anticipated)
Study Completion Date
June 30, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Vivantes Netzwerk für Gesundheit GmbH

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of the superiority study is to establish a reproducible, minimally invasive, cost-effective way of sample collection for microbiological and pathomorphological processing in a clinical setting with avoidance of anesthesia, multiple punctures, as well as potential deep contamination during irrigation.
Detailed Description
The main aim of the study is to demonstrate the superiority of a punch biopsy over a joint tap to rule out or prove septic prosthesis failure and thus establish a new diagnostic method. The subsequently calculated sensitivities of the previous and the procedure are used as the main indicator. In addition, we would like to prove that the total cost of diagnosing a septic / aseptic prosthesis failure using the proposed method has socio-economic advantages over the previous algorithm. One of the secondary objectives is the evaluation of the use of a punch biopsy for simultaneous a priori pathomorphological examination of periprosthetic soft tissue samples for the determination of wear particles. Furthermore, the study is intended to demonstrate a shortening of the time span between the first suspected diagnosis of septic prosthesis failure and its reliable exclusion / detection.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Wear of Articular Bearing Surface of Internal Prosthetic Joint, Infection Prosthetic, Infections Joint Prosthetic, Prosthetic Joint Infection, Prosthetic Pain
Keywords
prosthetic joint, infection, wear particles, prosthetic failure, antibiotics, biopsy, joint tap

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
132 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Joint tap
Arm Type
No Intervention
Arm Description
Joint tap and aspiration of synovial fluid
Arm Title
Punch biopsy
Arm Type
Experimental
Arm Description
Punch biopsy of a prosthetic joint and extraction of 5-7 biopsies from the synovial membrane
Intervention Type
Diagnostic Test
Intervention Name(s)
Punch biopsy
Intervention Description
A standardized biopsy kit is used for a synovial fluid tap and subsequent acquisition of up to 7 Punch biopsies through an introducer (part of the kit)
Primary Outcome Measure Information:
Title
Improved diagnostic accuracy
Description
Comparison of the specificity and sensibility of microbiological results for punch biopsies, the synovial fluid tap, pre-interventional blood Analysis, arthroscopic biopsies for confirmation/exclusion of a bacterial or fungal periprosthetic infection
Time Frame
up to 3 months
Secondary Outcome Measure Information:
Title
Rate of chronic periprosthetic low-grade-infections
Description
The incidence of hidden chronic periprosthetic infections
Time Frame
up to 3 Months
Title
Correlation of microbiological results from percutaneous Punch biopsy with intraoperative findings at Revision
Description
Correlation of pre-revision microbiological findings and the samples taken during the endoprosthesis replacement operation, in particular the sonicate of the prosthesis and the periprosthetic membrane (gold standard for infection diagnostics)
Time Frame
up to 6 Months
Title
Total Cost of Infection Diagnostics for various used methods
Description
Comparison of the respective Overall Costs for diagnostics of acute and chronic periprosthetic infections using a joint-tap, the novel punch biopsy method and arthroscopic biopsy
Time Frame
1 Month
Title
Rate of prosthetic failure due to wear particles
Description
Incidence of presence of wear particles in pathomorphological examinations of the punch biopsies and the samples taken during the replacement operation
Time Frame
up to 1 month
Title
Correlation of Synovialitis score and microbiological findings
Description
Correlation of Synovialitis score in pathomorphological examinations and microbiological verification of an acute or chronic periprosthetic infection
Time Frame
up to 2 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Preceding implantation of a shoulder, hip or knee endoprosthesis Acute or chronic pain in the joint Periprosthetic fracture Instability of the endoprosthesis Indications of wear / insufficiency of the enclosed plastic spacers Indications of metal abrasion Primary misalignment of the implant Exclusion Criteria: Confirmed periprosthetic infection Proven allergy to fast-acting local anesthetics
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rafal J Borucki, MD
Phone
+4915129211687
Email
rafal.borucki@vivantes.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karsten Labs, PD Dr
Organizational Affiliation
Vivantes Humboldt Krankenhaus
Official's Role
Study Chair
Facility Information:
Facility Name
Vivantes Humboldt-Krankenhaus
City
Berlin
ZIP/Postal Code
13509
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Karsten Labs, PD Dr. med.
Phone
+4930130121655
Email
karsten.labs@vivantes.de
First Name & Middle Initial & Last Name & Degree
Rafal J Borucki, MD
Phone
+4915129211687
Email
rafal.borucki@vivantes.de
First Name & Middle Initial & Last Name & Degree
Rafal J Borucki, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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Percutaneous Punch Biopsy for Diagnosis of Septic and Aseptic Prosthetic Joint Failure

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