N/A
N=1,439
Epidemiology of Severe Peroperative Bleeding During Scheduled Surgery
Surgery · Blood Loss
Bottom Line
View on ClinicalTrials.gov: NCT02311309 ↗Enrolled (actual)
1,439
Serious AEs
—
Results posted
Apr 2016
Primary outcome: Primary: Unanticipated Bleeding — 0; 100; 0 percentage of participants
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- Control (Other); Unanticipated bleeding (Other)
- Age
- Pediatric, Adult, Older Adult · 16+ yrs
- Sex
- All
- Sponsor
- University Hospital, Caen
- Primary completion
- Mar 2014
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Unanticipated Bleeding |
0; 100; 0 | — |
| SECONDARY Transfusions |
33; 31; 1; 508; 4; 862 | — |
| SECONDARY Preoperative Anemia |
— | — |
| SECONDARY Lowest Hemoglobin |
— | — |
Summary
Peroperative bleeding has been studied in specific populations exposed to bleeding (i.e. cardiac surgery, orthopedic surgery). Epidemiology of peroperative bleeding and transfusion remain poorly studied in the whole cohort of patients scheduled for surgery remain unknown. The investigators conducted a prospective study in order to examine the incidence, and risk factors associated with peroperative bleeding and transfusion.
Eligibility Criteria
Inclusion Criteria
- Patient scheduled for non cardiac and non emergency surgery
Exclusion Criteria
- Cardiac surgery
- Emergency surgery
Data sourced from ClinicalTrials.gov (NCT02311309). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.