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Capillary and Venous Blood Count Parameters

Comparison of Capillary and Venous Blood Count Parameters

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00390988
Enrollment
250
Registered
2006-10-23
Start date
Unknown
Completion date
Unknown
Last updated
2009-02-20

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

Conditions

Healthy Volunteers, Hematological Diseases

Keywords

blood count, capillary, venous, Adult, reference values

Brief summary

The purpose of this study is to compare capillary blood count parameters with the corresponding venous samples to verify the hypothesis that capillary and venous blood count parameters are equivalent.

Detailed description

In patients with haematological diseases regular blood count analyses are necessary. In haematology, capillary blood count analyses became established in routine diagnostics. The method and procedure of capillary blood sampling is well accepted by both the patients and the medical personal for a long time. However, only venous values are generally accepted in clinical routine. It is important to know whether or how capillary blood gives discrepant results for the various parameters. Values for therapeutic decisions, e.g. transfusion, are only known for venous values. So far, there are only deficient data available. Therefore, the aim of this study is (i) to compare capillary blood count parameters with the corresponding venous samples to verify the hypothesis that capillary and venous blood count parameters are equivalent, (ii) to include an adequate large number of adult haematological patients (with low and high values) and healthy adults, (iii) to obtain difference values for conversation of measured capillary values into the corresponding venous values.

Interventions

PROCEDUREblood sampling

Sponsors

University of Magdeburg
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients with haematological diseases ≥18 years * Healthy volunteers ≥18 years * Informed consent * No participation in another study 3 month before and during the study

Exclusion criteria

* Subjects \<18 years * Healthy subjects with acute or chronic infections and autoimmune or malignant diseases

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026