Early External Cephalic Version (ECV) 2 Trial

Status Completed

Clinical Trial Summary

For women with a fetus in breech presentation, does early ECV (at 34 0/7 up to 35 weeks and 6/7 days) versus delayed ECV (not before 37 weeks and 0/7 days) increase or decrease the likelihood of cesarean section (CS)?

Clinical Trial Description

Primary Outcomes: Rate of Caesarean section

Secondary Outcomes: Rate of preterm birth

Other Outcomes: admission to neonatal intensive care unit ≥ 24 hours, perinatal or neonatal mortality or serious neonatal morbidity, serious fetal complications, maternal death or serious maternal morbidity, non-cephalic presentation at birth, women's views, and health care costs.

The Data Coordination for this study is being carried out at the Maternal, Infant Reproductive Health Research Unit at Sunnybrook and Women's College Health Sciences Centre. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Breech Presentation

Clinical Trial Details

NCT number	NCT00141687
Study type	Interventional
Source	McMaster University
Contact
Status	Completed
Phase	N/A
Start date	December 2004
Completion date	June 2008

View Details

See also
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Terminated	`NCT00465712` - Effect of Amnioinfusion on External Cephalic Version Successful Rate	N/A
Recruiting	`NCT03827226` - Breech External Cephalic Version Intervention Trial
Completed	`NCT00813683` - Cephalic Version by Acupuncture for Breech Presentation	N/A
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