Clinical Trials Logo

Clinical Trial Summary

The aim of this study is to evaluate the effect of iohexol as a contrast agent on the anticoagulant activity of oral factor Xa inhibitors.


Clinical Trial Description

The study included 65 people who underwent contrast computerized tomography (CT). The study patients were divided into 4 groups. Patients in group 1 were using rivaroxaban (20 patients), patients in group 2 were using apixaban (20 patients), patients in group 3 were using edoxaban (20 patients), and group 4 was the control group (5 volunteers). Iohexol (60 ml) was used as a contrast agent. Two tubes were used to collect 2 ml of blood from the patients at 4 hours after the drug dose (rivaroxaban, apixaban, or edoxaban) and 1 hour after the contrast CT (CT was performed 3 hours after the drug was taken). In the control group, at any time and 1 hour after contrast CT, 2 tubes of 2 ml of blood were collected. The anticoagulant properties of rivaroxaban, apixaban, and edoxaban were evaluated using anti-factor Xa levels. ;


Study Design


Related Conditions & MeSH terms

  • Contrast Agents and Oral Factor Xa Inhibitor

NCT number NCT04611386
Study type Observational [Patient Registry]
Source Bursa Postgraduate Hospital
Contact
Status Completed
Phase
Start date January 1, 2019
Completion date August 1, 2019