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Clinical Trial Summary

Women at term (over 37 weeks) that are candidates for external cephalic version will be positioned in the trendelenburg position 5 minutes prior to external cephalic version performance and during the procedure. The control group will not be positioned differently than usual. We will evaluate external cephalic version success and compare the 2 groups.


Clinical Trial Description

This is a randomized controlled trial that is designed to compare external cephalic version success between women positioned in the trendelenburg position 5 minutes prior to external cephalic version performance and during the procedure and a control group of women that will lie on their back without special positioning. The women that are eligible for participation will receive a thorough explanation and will sign informed consent. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04585256
Study type Interventional
Source Rambam Health Care Campus
Contact Roy Lauterbach, MD
Phone +972-52-9432416
Email r_lauterbach@rmc.gov.il
Status Recruiting
Phase N/A
Start date November 1, 2020
Completion date December 31, 2023