Hemolysis in Blood Samples in the ER
1 other identifier
observational
2,800
1 country
1
Brief Summary
In this study, we aim to identify risk factors for hemolysis in blood samples drawn in the ED.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2013
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 19, 2013
CompletedFirst Posted
Study publicly available on registry
March 21, 2013
CompletedStudy Start
First participant enrolled
June 1, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2013
CompletedNovember 11, 2013
November 1, 2013
4 months
March 19, 2013
November 8, 2013
Conditions
Outcome Measures
Primary Outcomes (1)
Hemolysis rate
1 day
Study Arms (1)
ED patients
Eligibility Criteria
All adult (\> 16 y) patients admitted in the emergency departement during the study period
You may qualify if:
- \> 16 years
You may not qualify if:
- In vivo hemolysis
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Hospital, Geneva
Geneva, Canton of Geneva, 1211, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MD, MPH
Study Record Dates
First Submitted
March 19, 2013
First Posted
March 21, 2013
Study Start
June 1, 2013
Primary Completion
October 1, 2013
Study Completion
October 1, 2013
Last Updated
November 11, 2013
Record last verified: 2013-11