ChiCTR-TRC-12002644
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2012-11-04
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Breech Presentation during Pregnancy
External cephalic version for breech presentation: A randomised controlled trial of anaesthetic interventions
External cephalic version for breech presentation: A randomised controlled trial of anaesthetic interventions
Our objectives in this prospective randomised blinded control study are to compare the outcome and effects of using (A) intravenous analgesia or (B) spinal anaesthesia for primary and reattempts of ECV at term. Secondary objectives are comparisons of the effects on the fetus, mechanical forces used, pain and side effects during ECV. The conclusion will define the role of using IV analgesia and spinal anaesthesia for ECV, and establish guidelines that are not available in current literature.
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Random Shuffled coded envelope
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Research Grants Council of Hong Kong
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63
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2003-05-01
2008-10-01
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All singleton pregnancies suitable to have ECV for breech presentation at or beyond 36 weeks of gestation will be assessed for eligibility for inclusion. 24;25;27;40 ECVs for transverse lie, unstable lie, or second twin will be excluded for the purpose of this study. Patients suitable for this study would be in good health (ASA 1-2), and those contraindicated to have spinal anaesthesia or IV analgesia will be excluded. Informed written consent will obtained from all patients, before commencement of study.；
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