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NCT03516552 Clinical Trial

Comparison and Analysis of Blood Loss Formulas

Blood Loss Clinical Trial

Official title:
Comparison and Analysis of Blood Loss Formulas

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03516552
Other study ID # 2016/0906
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2018
Est. completion date August 10, 2018

Study information
Verified date August 2019
Source Hospital Clinic of Barcelona
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date August 10, 2018
Est. primary completion date July 30, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility 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.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Spain Hospital Clinic de Barcelona Barcelona

Sponsors (1)
Lead Sponsor Collaborator
Hospital Clinic of Barcelona

Country where clinical trial is conducted

Spain, 

Outcome
Type Measure Description Time frame Safety issue
Primary Differences on blood loss estimation. 72 hours.
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