RAI-IVDR23: Risk Analysis Interview IVDR 2023

Sponsor
Universitair Ziekenhuis Brussel (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06105086
Collaborator
Vrije Universiteit Brussel (Other)
30
1
1
7
4.3

Study Details

Study Description

Brief Summary

The objective of this research project is to design a risk-based model to decide when clinical performance studies should be performed on in-house developed in vitro diagnostic tests (IH-IVDs) in compliance with the European in vitro diagnostics regulation (EU IVDR 2017/746). To construct the dataset, semi-structured interviews will be conducted to assess the clinical hazards of the in-house in vitro diagnostic test assessments, their degree of significance and their importance with respect to clinical performance, as determined by the opinions of field specialists.

Condition or Disease Intervention/Treatment Phase
  • Other: Semi-structured interview
N/A

Detailed Description

The project's intervention involves conducting semi-structured interviews with clinical laboratory managers and medical professionals. The estimated number of participants for this study is 30. Various In-house in vitro diagnostic tests (IH-IVDs) will be selected, that are classified under different categories according to the risk management in the new IVDR. Two interviews will be conducted for each test. These interviews will engage a laboratory technician and a medical expert specialized in that particular test. The purpose of these interviews is to gather data on the variables that contribute to the risks of IH-IVDs and their impact on clinical diagnosis and patient outcomes. The obtained results will be applied in creating a decision tree using a pre-validated algorithm. The semi-structured interviews feature pre-determined questions that allow participants to share their experiences and opinions within their area of expertise. Each interview is expected to last between thirty minutes to an hour. If consent is given, the interviews will be recorded but not published or shared. In accordance with the confidentiality policy, all data collected will be kept anonymous.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Risk Analysis Interview IVDR 2023
Anticipated Study Start Date :
Dec 1, 2023
Anticipated Primary Completion Date :
Feb 20, 2024
Anticipated Study Completion Date :
Jun 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: medical doctors and clinical laboratory managers

Semi-structured interviews

Other: Semi-structured interview
Participants will be asked pre-defined questions and are allowed to elaborate on the subject.

Outcome Measures

Primary Outcome Measures

  1. Risk attributes of the in-house in vitro diagnostic tests measured with semi-structured interviews [1 hour]

    Risk attributes of the in-house in vitro diagnostic tests are the variables that have an impact on the clinical diagnosis and patient outcome. This will be measured with a semi-structured interview with medical doctors and laboratory managers.

  2. risk impact of the in-house in vitro diagnostic tests measured with semi-structured interviews [1 hour]

    With the opinions and experience of professionals in the field of interest, the risk impact of the in-house in vitro diagnostic tests will be measured with semi-structured interviews. The impact defines the severity or importance of the risk attributes.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Work relation with the medical field/hospital

  • Achieved a master degree or higher

  • Compatible to take an interview independently

Exclusion Criteria:

/

Contacts and Locations

Locations

Site City State Country Postal Code
1 UZ brussel Brussels Belgium 1090

Sponsors and Collaborators

  • Universitair Ziekenhuis Brussel
  • Vrije Universiteit Brussel

Investigators

  • Principal Investigator: Johan Guns, Prof., UZ Brussel Laboratorium Kwaliteit

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Johan Guns, Prof., Universitair Ziekenhuis Brussel
ClinicalTrials.gov Identifier:
NCT06105086
Other Study ID Numbers:
  • 23353_RAI-IVDR23
First Posted:
Oct 27, 2023
Last Update Posted:
Oct 27, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Johan Guns, Prof., Universitair Ziekenhuis Brussel

Study Results

No Results Posted as of Oct 27, 2023