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NCT01815931 Clinical Trial

Hemolysis in Blood Samples in the ER

Emergencies Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01815931
Other study ID # SU-032013
Secondary ID
Status Completed
Phase N/A
First received March 19, 2013
Last updated November 8, 2013
Start date June 2013
Est. completion date October 2013

Study information
Verified date November 2013
Source University Hospital, Geneva
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Observational

Clinical Trial Summary

In this study, we aim to identify risk factors for hemolysis in blood samples drawn in the ED.

Recruitment information / eligibility
Status Completed
Enrollment 2800
Est. completion date October 2013
Est. primary completion date October 2013
Accepts healthy volunteers No
Gender Both
Age group 16 Years and older
Eligibility Inclusion Criteria:

- > 16 years

Exclusion Criteria:

- In vivo hemolysis

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Switzerland University Hospital, Geneva Geneva GE

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Geneva

Country where clinical trial is conducted

Switzerland, 

Outcome
Type Measure Description Time frame Safety issue
Primary Hemolysis rate 1 day No
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