Improved Intraoperative Blood Loss Estimates Clinical Trial
— EBLOfficial title:
Method for Improved Intraoperative Blood Loss Estimates
| NCT number | NCT01634828 |
| Other study ID # | FP00002762 |
| Secondary ID | 56181 |
| Status | Recruiting |
| Phase | N/A |
| First received | July 2, 2012 |
| Last updated | July 5, 2012 |
| Start date | July 2012 |
| Verified date | July 2012 |
| Source | University of Utah |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Institutional Review Board |
| Study type | Observational |
The purpose of this study is to develop a mathematical algorithm which the investigators plan to use to more accurately estimate intraoperative blood loss.
| Status | Recruiting |
| Enrollment | 50 |
| Est. completion date | |
| Est. primary completion date | |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: All elective surgical patients Exclusion Criteria: 1. Age < 18 2. Pregnant women 3. Prisoners 4. Lack of informed consent 5. Attending Physician feels enrollment could interfere with optimal patient care 6. Patients who did not have a preoperative hemoglobin measured as part of their preoperative work-up 7. Patients whose preoperative hemoglobin fraction is abnormal. 8. Patients who will likely require an intraoperative blood transfusion. 9. Patients for whom the intraoperative use of the Cell Saver is anticipated. |
Observational Model: Cohort, Time Perspective: Prospective
| Country | Name | City | State |
|---|---|---|---|
| United States | University of Utah | Salt lake City | Utah |
| Lead Sponsor | Collaborator |
|---|---|
| University of Utah |
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