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Study on the application of epidural block for labor analgesia under the guidance of ultrasound

Study on the application of epidural block for labor analgesia under the guidance of ultrasound

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072727
Enrollment
Unknown
Registered
2023-06-22
Start date
2023-06-12
Completion date
Unknown
Last updated
2023-06-26

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:Epidural block for spinal cord perforation
EP group:Simple epidural block

Sponsors

The first People's Hospital of Huai'an, Huai'an attached to the Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. single full-term primipara to be delivered via vagina; 2. age 20-40 years; 3. ASA class i-II; 4. 18.5= BMI < 30kg/m2; 5. fetal heart rate monitoring was normal before delivery.

Exclusion criteria

Exclusion criteria: 1. contraindication of epidural puncture; 2. those who were confirmed by obstetrician as unsuitable for vaginal trial labor; 3. Delayed or rapid delivery; 4. dysfunction of heart and lung; 5. persons with allergic history of related drugs used by research institute; 6. patients with mental disorders; 7. Have a history of drug or alcohol addiction.

Design outcomes

Primary

MeasureTime frame
VAS;

Secondary

MeasureTime frame
First press time of self-control analgesia pump;Consumption of Ropivacaine and sufentanil;PCA Press Times;IL-6 and TNF in serum- a Expression level of;Satisfaction rating;

Countries

China

Contacts

Public Contactwangyun

The first People's Hospital of Huai'an, Huai'an attached to the Nanjing Medical University

2858093166@qq.com+86 157 2287 5256

Outcome results

None listed

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