Skip to content

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

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04253093
Enrollment
50
Registered
2020-02-05
Start date
2019-08-01
Completion date
2020-12-01
Last updated
2020-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy Related

Brief 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.

Interventions

None listed

Sponsors

Hallym University Kangnam Sacred Heart Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 45 Years

Inclusion criteria

* women undergoing general anesthesia

Exclusion criteria

* liver disease * renal disease * diabetes mellitus * asthma * allergic to specific drugs * BMI\>30 or \<18

Design outcomes

Primary

MeasureTime frameDescription
duration of rocuroniumtime measured to 25% recovery with T1 using Train of Four watch, assessed upto 1 hourtime measured with TOFwatch-SX

Secondary

MeasureTime frameDescription
onset of rocuroniumtime measured to 0% depression of T1 using Train of Four watch, assessed upto 5 minutestime measured with TOFwatch-SX

Countries

South Korea

Contacts

Primary ContactInJung Jun
christine17@hanmail.net82-10-9312-0162

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026