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Application of combined spinal-epidural anesthesia with ropivacaine on the external cephalic version

Application of combined spinal-epidural anesthesia with ropivacaine on the external cephalic version

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200059856
Enrollment
Unknown
Registered
2022-05-13
Start date
2022-05-01
Completion date
Unknown
Last updated
2024-04-08

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

Conditions

External cephalic version

Interventions

Group S:None
Group M:None
Group L:None

Sponsors

Fujian Maternity and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. 37 to 40 weeks of gestation; 2. Singleton pregnancy, breech presentation; 3. Willing to receive combined spinal-epidural analgesia for external cephalic version.

Exclusion criteria

Exclusion criteria: 1. There are contraindications of intraspinal anesthesia; 2. Allergy to any study medication; 3. Uterine malformation; 4. History of cesarean section; 5. Patients with contraindications of vaginal delivery.

Design outcomes

Primary

MeasureTime frame
The success rate of external cephalic version;—

Secondary

MeasureTime frame
Duration of external cephalic version;Blood pressure;Heart Rate;Use of vasoactive drugs;—

Countries

China

Contacts

Public ContactPeihan Xiao

Fujian Maternity and Child Health Hospital

279966838@qq.com+86 13696853855

Outcome results

None listed

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