Actively Recruiting

Age: 18Years +
All Genders
NCT06416280

Inter-observer Reliability of the TRiP(Cast) Score in Patients With Trauma to a Lower Limb Requiring Immobilisation

Led by University Hospital, Angers · Updated on 2024-05-17

302

Participants Needed

1

Research Sites

84 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of the study isto evaluate the inter-observer reliability of the assessment of venous thromboembolic risk using the TRiP(cast) score in patients presenting with trauma to a lower limb requiring immobilisation, and of the clinicians' assessment using the physician's implicit probability (gestalt) compared with the use of the TRiP(cast) score.

CONDITIONS

Official Title

Inter-observer Reliability of the TRiP(Cast) Score in Patients With Trauma to a Lower Limb Requiring Immobilisation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Consultation in one of the emergency departments participating in the study
  • Isolated trauma to a lower limb
  • Rigid immobilisation (plaster or resin) or semi-rigid immobilisation for an expected duration of at least 7 days
  • Patient over 18 years of age
  • Patient affiliated to or benefiting from a social security scheme
  • Patients who have signed a prior informed consent form
Not Eligible

You will not qualify if you...

  • Patient taking anticoagulant treatment at the time of the trauma
  • Trauma requiring hospitalisation for more than 48 hours
  • Pregnant, breast-feeding or parturient patients
  • Patient deprived of liberty by judicial or administrative decision
  • Patient under compulsory psychiatric care
  • Patient under legal protection
  • Patients unable to give their free and informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

DOUILLET Delphine

Angers, France

Actively Recruiting

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Research Team

D

Delphine DOUILLET

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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