ClinicalTrials.Veeva

Menu

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

H

Hallym University Kangnam Sacred Heart Hospital

Status

Unknown

Conditions

Pregnancy Related

Study type

Observational

Funder types

Other

Identifiers

NCT04253093
2019-05-008

Details and patient eligibility

About

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

Full 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.

Enrollment

50 estimated patients

Sex

Female

Ages

20 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • women undergoing general anesthesia

Exclusion criteria

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

Trial contacts and locations

1

Loading...

Central trial contact

InJung Jun

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems