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Clinical Trial Summary

A comparison of external cephalic (ECV) success rates when ECV performed with full urinary bladder or not. The study is prospective and randomised. Both nulliparous and multiparous women will be enrolled in the study, however each group will be randomized separately either to full urinary bladder or not. Written informed consent will be obtained prior to inclusion in the study.


Clinical Trial Description

A comparison of external cephalic (ECV) success rates when ECV performed with full urinary bladder or not. The study is prospective and randomised. Both nulliparous and multiparous women will be enrolled in the study, however each group will be randomized separately either to full urinary bladder or not. Written informed consent will be obtained prior to inclusion in the study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04118465
Study type Interventional
Source Hadassah Medical Organization
Contact
Status Completed
Phase N/A
Start date January 2002
Completion date December 31, 2020

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