Evaluation of microsampling systems for bloodanalysis in the follow-up of patients

Completed

• Conditions: diagnostiek; Preanalytical procudures for bloodsampling

• Registration Number: NL-OMON49860
• Lead Sponsor: Medlon b.v. Medische Diagnostiek

Brief Summary

Trial ended prematurely

Detailed Description

Not available

Study Timeline

• Study Completion: 2024-06-01
• Last Update Posted: 18 June 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 80

Inclusion Criteria

Patients from the outpatient clinic
Aged above 18 years
Informed consent

Exclusion Criteria

Unable to read and understand patientinformation.

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Effect of capillaire sampling in buffersolution and kept at roomtemperature on<br /><br>23 laboratory parameters.In this study the outcome of different tests (CRP,<br /><br>ALAT, Albumine, Alkalisch fosfatase, Amylase, ASAT, Cholesterol, Kreatinine,<br /><br>Ferritine, Immunoglobulines, IJzer, Gamma-GT, HbA1c, HDL cholesterol, LDL<br /><br>Cholesterol, Apolipoproteine B, Totaal Eiwit, Transferrine, Triglycerides, TSH,<br /><br>Holotranscobalamine, Foliumzuur, Hemoglobin, Leucocytes, Trombocytes, LD and<br /><br>NT-proBNP) will be evaluated between blood drawn by venapuncture and capillary<br /><br>blood (capillary blood kept in Hem-Col tubes for 72 hrs).<br /><br>Results of these tests (blood drawn by venapuncture) will be reported to their<br /><br>physician. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Participants experience of capillary sampling.</p><br>