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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.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002644
Enrollment
Unknown
Registered
2012-11-04
Start date
2003-05-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breech Presentation during Pregnancy

Interventions

None listed

Sponsors

Research Grants Council of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 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.

Exclusion criteria

Exclusion criteria: NA

Design outcomes

Primary

MeasureTime frame
Successful ECV;—

Countries

China

Contacts

Public ContactKHAW Kim Sun
kimkhaw@gmail.com+852 26322735

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026