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Evaluation of new blood collection systems

Completed
Conditions
geen enkele. De proefpersonen worden niet op aandoening geselecteerd.
none
Registration Number
NL-OMON48834
Lead Sponsor
Medlon b.v.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
110
Inclusion Criteria

healthy volunteer or
patients attending the outpatient clinic

Exclusion Criteria

patient with known anemia

Study & Design

Study Type
Observational invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Comparison of labresults obtained with the regular collecting system or the new<br /><br>one.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>n.a.</p><br>
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