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
| Type | Name | Description |
|---|---|---|
| OTHER | Plasmalyte-148 | Venous 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.