Clinical Trials Directory

Trials / Suspended

SuspendedNCT03797833

Spinal Anesthesia for External Cephalic Version

Spinal Anesthesia for External Cephalic Version in Nulliparous Women, A Controlled Randomized Study

Status
Suspended
Phase
N/A
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Region Skane · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study evaluates the potential benefits of spinal anaesthesia for nulliparous mothers scheduled for external version of babies in breech position.

Detailed description

Fetuses in breech position are almost always delivered by Caesarian section (CS). If the fetus is in breech position by the end of pregnancy, attempts for external cephalic version (ECV) are usually made. The success rate of ECV in nulliparous women is lower than in multiparous women. There are studies showing a higher rate of successful ECV's if the mother received a low dose spinal anaesthesia (SA). Overall maternal satisfaction was higher with SA. These studies, however, did not take parity into account. The primary aim of this study is to see if SA can increase the rate of successful ECV's in nulliparous women. The secondary aims are to evaluate if maternal satisfaction increases and if the rate of CS is decreasing using SA during ECV.

Conditions

Interventions

TypeNameDescription
PROCEDURESpinal AnaesthesiaSpinal anaesthesia with Bupivacain 2.5 mg and Sufentanil 5 µg

Timeline

Start date
2019-01-07
Primary completion
2029-01-31
Completion
2030-06-30
First posted
2019-01-09
Last updated
2022-10-27

Locations

2 sites across 1 country: Sweden

Source: ClinicalTrials.gov record NCT03797833. Inclusion in this directory is not an endorsement.