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Clinical Trials/NCT01634828
NCT01634828
Completed
Not Applicable

Method for Improved Intraoperative Blood Loss Estimates

University of Utah1 site in 1 country47 target enrollmentJuly 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Improved Intraoperative Blood Loss Estimates
Sponsor
University of Utah
Enrollment
47
Locations
1
Primary Endpoint
Estimate of intraoperative blood loss
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to develop a mathematical algorithm which the investigators plan to use to more accurately estimate intraoperative blood loss.

Registry
clinicaltrials.gov
Start Date
July 2012
End Date
April 2015
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Annette Macintyre

Principle Investigator

University of Utah

Eligibility Criteria

Inclusion Criteria

  • All elective surgical patients

Exclusion Criteria

  • Pregnant women
  • Lack of informed consent
  • Attending Physician feels enrollment could interfere with optimal patient care
  • Patients who did not have a preoperative hemoglobin measured as part of their preoperative work-up
  • Patients whose preoperative hemoglobin fraction is abnormal.
  • Patients who will likely require an intraoperative blood transfusion.
  • Patients for whom the intraoperative use of the Cell Saver is anticipated.

Outcomes

Primary Outcomes

Estimate of intraoperative blood loss

Time Frame: duration of surgery

Study Sites (1)

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