Skip to content

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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON49860
Enrollment
80
Registered
2019-11-04
Start date
2020-01-14
Completion date
Unknown
Last updated
2024-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

diagnostiek Preanalytical procudures for bloodsampling

Interventions

None listed

Sponsors

Medlon b.v. Medische Diagnostiek
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients from the outpatient clinic Aged above 18 years Informed consent

Exclusion criteria

Exclusion criteria: Unable to read and understand patientinformation.

Design outcomes

Primary

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

Secondary

MeasureTime frame
Participants experience of capillary sampling.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)