MedTrace Logo

Spinal Anesthesia for External Cephalic Version

NCT03797833 · Status: SUSPENDED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2022-10-27

No results posted yet for this study

Summary

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

Conditions

  • Breech Presentation; Before Labor

Interventions

PROCEDURE

Spinal Anaesthesia

Spinal anaesthesia with Bupivacain 2.5 mg and Sufentanil 5 µg

Sponsors & Collaborators

  • Region Skane

    lead OTHER

Principal Investigators

  • Andreas Herbst, MD PhD · Lund University, IKVL gyn/ob . Skåne University Hospital, Lund Sweden

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-07
Primary Completion
2029-01-31
Completion
2030-06-30

Countries

  • Sweden

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03797833 on ClinicalTrials.gov