Clinical Trials Directory

Trials / Completed

CompletedNCT04093479

Impact of Maternal BMI on Plasma Levels of Oxytocin During Labor Augmentation

Status
Completed
Phase
Study type
Observational
Enrollment
40 (actual)
Sponsor
Linkoeping University · Other Government
Sex
Female
Age
18 Years
Healthy volunteers

Summary

The aim of this study is to examine the associations between maternal BMI and levels of oxytocin in maternal plasma during augmentation with oxytocin during first stage of labor in term pregnancy.

Detailed description

A translational prospective experimental study in the delivery ward in Linköping. The study population will include women in two BMI groups (underweight/normal weight and overweight/obese) during first stage of labor with singleton full term pregnancy and cephalic presentation.The BMI is calculated from weight and height registered at the first antenatal visit around week 8-12. At the delivery ward, if the women are in need of labor augmentation with oxytocin infusion, a peripheral venous catheter will be placed in the contralateral arm from the arm where oxytocin will be administrated. The oxytocin infusion will be prepared to a concentration of 10 mU/ml and will be given according to a standardized protocol or to an infusion level giving maximum of 5 uterine contractions per 10 minutes. Blood samples for measuring plasma levels of oxytocin will be taken prior to start and before every increase in the rate of oxytocin infusion. The blood samples will be collected through the first stage of labor.

Conditions

Interventions

TypeNameDescription
OTHERblood samplesblood samples will be taken repeatedly

Timeline

Start date
2019-10-01
Primary completion
2019-12-01
Completion
2020-08-01
First posted
2019-09-18
Last updated
2021-02-21

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT04093479. Inclusion in this directory is not an endorsement.