Dexmedetomidine and Blood Coagulation
NCT04269278 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 11
Last updated 2021-07-02
Summary
Dexmedetomidine may alter whole blood coagulation. However, little is known about the dose-response relationships according to the blood concentration of dexmedetomidine. The investigators have therefore performed the present study to measure the effect of dexmedetomidine on the coagulation pathway according to the drug concentration level using a rotational thromboelastometry test.
Conditions
- Blood Coagulation Disorder
Interventions
- DRUG
-
0 ul of dexmedetomidine
Venous blood is taken from 11 healthy volunteers and divided into four specimen bottles, which were added with different doses (0 ul) using dexmedetomidine
- DRUG
-
0.25 ul of dexmedetomidine
Venous blood is taken from 11 healthy volunteers and divided into four specimen bottles, which were added with different doses (0.25 ul) using dexmedetomidine
- DRUG
-
0.5 ul of dexmedetomidine
Venous blood is taken from 11 healthy volunteers and divided into four specimen bottles, which were added with different doses (0.5 ul) using dexmedetomidine
- DRUG
-
0.75 ul of dexmedetomidine
Venous blood is taken from 11 healthy volunteers and divided into four specimen bottles, which were added with different doses (0.75 ul) using dexmedetomidine
Sponsors & Collaborators
-
Seoul National University Bundang Hospital
lead OTHER
Principal Investigators
-
Hyo-Seok Na, MD., PhD. · Seoul National University Bundang Hospital
Eligibility
- Min Age
- 20 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2020-02-12
- Primary Completion
- 2020-12-30
- Completion
- 2020-12-30
Countries
- South Korea
Study Locations
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