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Dutch Fracture Infection Registry

Long term outcome after fracture-related infection: The Dutch Fracture Infection Registration Subtitel: Protocol for a multicentre prospective cohort registration study of patients with a fracture-related infection.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON25812
Enrollment
1000
Registered
2020-05-21
Start date
2020-07-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fracture Related Infection (FRI)

Interventions

None (observational registry for future research)

Sponsors

University Medical Centre Utrecht & university Medical Centre Groningen
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: In order to be eligible to be included in the DFIR, a subject must be >15 years and undergoing investigation and/or treatment (operative or non-operative) and/or follow-up for a proven or suspected FRI in one of the participating centres. FRI or suspected FRI is defined according to the FRI consensus definition (REF: Metsemaker et al, Injury 2018). This definition consists of definite signs (FRI present) and suggestive signs (FRI suspected). Both types of signs qualify for inclusion,and both early (onset 6 weeks after fracture operation) can be included.

Exclusion criteria

Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: • Fracture patients with an unremarkable postoperative course • Age < 16 years • Expected inability to meet at least 1 year follow-up • No Dutch or English proficiency

Design outcomes

Primary

MeasureTime frame
None (observational registry for future research)

Secondary

MeasureTime frame
None (observational registry for future research)

Contacts

Public ContactDr. G.A.M. Govaert

UMC Utrecht

g.a.m.govaert@umcutrecht.nl+31887559882

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)