Capillary and Venous Blood Count Parameters

This study has been completed.
Sponsor:
Information provided by:
University of Magdeburg
ClinicalTrials.gov Identifier:
NCT00390988
First received: October 20, 2006
Last updated: February 19, 2009
Last verified: February 2009
  Purpose

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.


Condition Intervention
Hematological Diseases
Healthy Volunteers
Procedure: blood sampling

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Comparison of Capillary and Venous Blood Count Parameters

Resource links provided by NLM:


Further study details as provided by University of Magdeburg:

Estimated Enrollment: 250
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.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00390988

Sponsors and Collaborators
University of Magdeburg
Investigators
Principal Investigator: Kathleen Jentsch-Ullrich, Dr. University Hospial Magdeburg, Division of Haematoloy/Oncology, Leipziger Str. 44, D-39120 Magdeburg, Germany
  More Information

Publications:
ClinicalTrials.gov Identifier: NCT00390988     History of Changes
Other Study ID Numbers: MD FME 45/06
Study First Received: October 20, 2006
Last Updated: February 19, 2009
Health Authority: Germany: Ethics Commission

Keywords provided by University of Magdeburg:
blood count
capillary
venous
Adult
reference values

Additional relevant MeSH terms:
Hematologic Diseases

ClinicalTrials.gov processed this record on September 14, 2014