Clinical Trials Directory

Trials / Unknown

UnknownNCT04253093

Comparison of Rocuronium Induced Neuromuscular Blockade in Late Second Trimester Pregnant and Non-pregnant Women

Status
Unknown
Phase
Study type
Observational
Enrollment
50 (estimated)
Sponsor
Hallym University Kangnam Sacred Heart Hospital · Academic / Other
Sex
Female
Age
20 Years – 45 Years
Healthy volunteers

Summary

The present study is to compare the onset and duration of rocuronium in late second trimester women and non-pregnant women undergoing general anesthesia.

Detailed description

Pregnancy induces physiological changes. Plasma volume, cardiac output, hepatic blood flow and protein binding are changed from the first trimester of pregnancy. These physiological changes give effect to the onset and duration of neuromuscular blocking drugs. Rocuronium is a commonly used neuromuscular blocking drug categorized as FDA category B. Rocuronium is widely used for pregnant women. Previous studies have evaluated the onset and duration of rocuronium in postpartum women. Lately, the investigators have evaluated the onset and duration of rocuronium in early second trimester pregnant women and the duration was significantly longer in early second trimester women compared to non-pregnant women. Since there is little research on the onset and duration of rocuronium in the late second trimester pregnant women, the investigators planned the present research.

Conditions

Timeline

Start date
2019-08-01
Primary completion
2020-10-01
Completion
2020-12-01
First posted
2020-02-05
Last updated
2020-02-05

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT04253093. Inclusion in this directory is not an endorsement.