Hemolysis in Blood Samples in the ER

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

Completed

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Key information

Conditions

Hemolysis Blood Specimen Collection Disease Attributes Emergencies Emergency Service, Hospital Pathologic Processes Pathological Conditions, Signs and Symptoms

Age range

16 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital, Geneva

Geneva, Canton of Geneva, 1211, Switzerland

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

> 16 years

Exclusion criteria

In vivo hemolysis

Treatment and study plan

Primary outcomes

Hemolysis rate

Time frame: 1 day

Sponsors and collaborators

Lead sponsor

University Hospital, Geneva

Other

Registry information

Important dates

Study start: 2013
Primary completion: 2013
Study completion: 2013
First posted: Mar 21, 2013
Registry last updated: Nov 11, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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