Clinical Trials Directory

Trials / Completed

CompletedNCT03168087

Plasmalyte-148 Solution and Blood Coagulation

The Effect of a Plasmalyte-148 Solution on Blood Coagulation: In Vitro, Volunteer Study Using Rotational Thromboelastometry

Status
Completed
Phase
Study type
Observational
Enrollment
12 (actual)
Sponsor
Seoul National University Hospital · Academic / Other
Sex
All
Age
20 Years – 65 Years
Healthy volunteers
Accepted

Summary

Fluids administered intravenously may alter whole blood coagulation. However, little is known about the dose-response relationships of hemodilution in plasmalyte-148 solution. Investigators have therefore performed the present study to measure the effect of a plasmalyte-148 solution on the coagulation pathway according to the hemodilution level using a rotational thromboelastometry (ROTEM®) tests.

Conditions

Interventions

TypeNameDescription
OTHERPlasmalyte-148Venous blood is taken from 12 healthy volunteers and divided into four specimen bottles, which were diluted with different levels (0%, 20%, 40%, and 60%) using a plasmalyte-148 solution.

Timeline

Start date
2017-05-15
Primary completion
2018-08-23
Completion
2018-08-30
First posted
2017-05-30
Last updated
2020-02-13

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03168087. Inclusion in this directory is not an endorsement.