Actively Recruiting

All Genders
NCT05254353

Comparison of Different CSF Sampling Sites on External Ventricular Drains

Led by Universitaire Ziekenhuizen KU Leuven · Updated on 2024-07-01

55

Participants Needed

1

Research Sites

152 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of the current study is to evaluate the difference between proximal and distal CSF sampling. If the characteristics of distally and proximally sampled CSF are similar or correlate well, it may be possible to only sample CSF distally in the future, thereby avoiding the risks mentioned above.

CONDITIONS

Official Title

Comparison of Different CSF Sampling Sites on External Ventricular Drains

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with an external ventricular drain (EVD) in place regardless of the underlying pathology
  • Written informed consent obtained from the patient or a legally acceptable representative
  • If the patient is capable but physically unable to sign, an impartial witness can attend the consent process
  • Males and females of all ages, including children and pregnant females
Not Eligible

You will not qualify if you...

  • Patients scheduled to have the external ventricular drain removed within 48 hours before routine sampling

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

UZ Leuven

Leuven, Belgium, 3000

Actively Recruiting

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Research Team

P

Philippe De Vloo, prof.dr.

CONTACT

T

Tom Deleu, dr.

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

1

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