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Clinical study of dural puncture epidural in cesarean section

Clinical study of dural puncture epidural in cesarean section

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052541
Enrollment
Unknown
Registered
2021-10-30
Start date
2021-11-10
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Cesarean section

Interventions

Epidural group:Epidural anesthesia
Combined spinal epidural anesthesia group:Combined spinal epidural anesthesia
Dural puncture epidural block group:Dural puncture epidural

Sponsors

Yichang Central People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Singleton full-term pregnant women who intend to undergo cesarean section; 2. Aged 20 to 40 years; 3. ASA grade I-II; 4. The patient signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Body mass index >= 35kg/m2; 2. Serious cardiovascular and cerebrovascular diseases; 3. Liver and kidney dysfunction; 4. Hypertension during pregnancy; 5. Severe anemia; 6. Fetal distress in utero; 7. Abnormal coagulation and infection of puncture site with contraindications to spinal anesthesia.

Design outcomes

Primary

MeasureTime frame
Sensory block plane;Degree of lower extremity motor nerve block;—

Secondary

MeasureTime frame
Postoperative intestinal exhaust time;Motor nerve recovery time;Vital signs;—

Countries

China

Contacts

Public ContactGong Yuan

Yichang Central People's Hospital

y-yc@163.com+86 13986746821

Outcome results

None listed

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