NCT01815931CompletedNot Applicable
Hemolysis in Blood Samples in the ER
University Hospital, Geneva1 site in 1 country2,800 target enrollmentStarted: June 2013Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- University Hospital, Geneva
- Enrollment
- 2,800
- Locations
- 1
- Primary Endpoint
- Hemolysis rate
Study Overview
Brief Summary
In this study, we aim to identify risk factors for hemolysis in blood samples drawn in the ED.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 16 Years to — (Child, Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •> 16 years
Exclusion Criteria
- •In vivo hemolysis
Outcomes
Primary Outcomes
Hemolysis rate
Time Frame: 1 day
Secondary Outcomes
No secondary outcomes reported
Investigators
Olivier T. Rutschmann
MD, MPH
University Hospital, Geneva
Study Sites (1)
Loading locations...
Similar Trials
Unknown
Not Applicable
Pilot Bleeding Study: Risk and Protective Factors Associated With Bleeding in the Hemodialysis PopulationBleedingEnd Stage Renal DiseaseNCT00182117Hamilton Health Sciences Corporation490
Completed
Not Applicable
Platelet Function in Hemodialysis PatientChronic Kidney DiseaseNCT02792283CHU de Reims100
Completed
Not Applicable
Long Term Effects of Erythrocyte LysisSickle Cell DiseaseHemolytic AnemiaNCT00842621St. Jude Children's Research Hospital390
Completed
Not Applicable
Accelerated Mortality on Renal ReplacementEnd Stage Renal DiseaseNCT00505180Massachusetts General Hospital10,018
Completed
Not Applicable
Blood Collection of Patient Presenting in the ED and Prescribed a BNPHeart FailureNCT02614209Fujirebio Diagnostics, Inc.400