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Detection of neonatal sepsis using dynamic light scattering skin sensors

Recruiting
Conditions
neonatale sepsis
blood poisoning
sepsis
Registration Number
NL-OMON54452
Lead Sponsor
Erasmus MC, Universitair Medisch Centrum Rotterdam
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
32
Inclusion Criteria

- Suspicion of late-onset sepsis
- Written informed consent of parents or guardian
- Blood culture is drawn

Exclusion Criteria

- Skin disorder (including frailty of the skin) for which the skin adhesive is
contraindicated

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The main study endpoint is the microcirculatory red blood cell velocity<br /><br>measured with the dynamic light scattering sensor in neonates during sepsis<br /><br>compared to neonates in whom sepsis is not proven.</p><br>
Secondary Outcome Measures
NameTimeMethod
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