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Study on the safety and effectiveness of ultrasound-guided dura puncture epidural block in labor analgesia

Study on the safety and effectiveness of ultrasound-guided dura puncture epidural block in labor analgesia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300067438
Enrollment
Unknown
Registered
2023-01-09
Start date
2023-01-09
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

labor pain

Interventions

DPE group:Dural puncture epidural analgesia
EP group:Traditional epidural analgesia

Sponsors

Xuzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Full term primiparas of single fetus who plan to deliver vaginally; 2. Age 20-40; 3. ASA Grade I-II; 4. 18.5=BMI < 35.5kg/m2 5. Fetal heart monitoring is normal before delivery

Exclusion criteria

Exclusion criteria: 1. Patients with contraindications to epidural puncture; 2. Those who have been confirmed by an obstetrician that vaginal birth is not suitable; 3. Delayed or urgent labor; 4. Dysfunction of important organs such as heart and lung; 5. Have a history of allergy to all related drugs; 6. People with mental illness; 7. A history of drug or alcohol addiction;

Design outcomes

Primary

MeasureTime frame
Probability of VAS score =1 during contraction 10 minutes after initial epidural catheter infusion;

Secondary

MeasureTime frame
First PCA time;Number of PCA presses;Consumption of ropivacaine and sufentanil;

Countries

China

Contacts

Public ContactWang Liwei

Xuzhou Central Hospital

doctorlww@sina.com18952170255

Outcome results

None listed

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