Clinical Trials Logo

Clinical Trial Summary

This study aimed to determinate effective dose 95 (ED95) intravenous cannulation in pediatric patient after induction of sevoflurane 8 vol%


Clinical Trial Description

Twenty-two subjects were given informed consent before study enrolled. Anesthesia was induced by 8% sevoflurane with 6 L flow of 100% oxygen. IV cannulation was attempted at 2 min in the first child in each group. The time for cannulation in the next child was stepped up or down by 15 s depending on positive or negative response, respectively, in the previous child. Children were recruited till a minimum of six pairs of failure-success sequence which was obtained in the group. The mean of midpoints of the failure-success sequence was calculated to obtain the time for cannulation in 50% of the group. ;


Study Design


Related Conditions & MeSH terms

  • Movement After Intravenous Cannulation

NCT number NCT04284579
Study type Interventional
Source Indonesia University
Contact
Status Completed
Phase N/A
Start date May 27, 2019
Completion date November 30, 2019