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Comparison and Analysis of Blood Loss Formulas

H

Hospital Clinic of Barcelona

Status

Completed

Conditions

Blood Loss

Study type

Observational

Funder types

Other

Identifiers

NCT03516552
2016/0906

Details and patient eligibility

About

Although it has been pointed that estimates are significantly inexact and different from each other, the actual accuracy of them has not been properly investigated and compared.

Enrollment

100 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults 18 - 90 yrs.

Exclusion criteria

  • Suspected or confirmed coagulopathy (including current treatment with anticoagulants or antiplatelet agents).
  • Surgical blood loss volume < 200 ml.
  • Requirement for surgical gauzes during surgery, including conversion to open surgical techniques.
  • Transfusion of red blood cells (RBCs) during the perioperative period.
  • Significant postoperative bleeding (> 50 ml in surgical drains) or any other type of significant blood loss.
  • Fluid infusions or vasoactive drugs after the first 24 postoperative hours.

Trial design

100 participants in 1 patient group

Hemoglobin content on blood loss
Description:
Hemoglobin content on blood loss, to assess ratio hemoglobin/volume.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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