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To explore the analgesic management model of different types of parturients in vaginal delivery

To explore the analgesic management model of different types of parturients in vaginal delivery

Status
Unknown
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086762
Enrollment
Unknown
Registered
2024-07-10
Start date
2024-05-15
Completion date
Unknown
Last updated
2025-09-29

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

Conditions

painless childbirth

Interventions

I group: 0.08%Ropivacaine + Sufentanil 5ug
II group:0.09%Ropivacaine + Sufentanil 5ug
III group:0.1%Ropivacaine + Sufentanil 5ug

Sponsors

Yunnan First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: Age 22-34 years old, gestational age 37-41 weeks, single pregnancy, normal maternal and fetal indicators, and informed consent from both maternal and family members;

Exclusion criteria

Exclusion criteria: Patients with primary uterine atony, misaligned fetal position, history of severe cardiovascular and pulmonary diseases, allergies to local anesthetics and opioids, contraindications to spinal anesthesia, conversion to cesarean section, or prolonged delivery time (>10 hours).

Design outcomes

Primary

MeasureTime frame
pain score;

Secondary

MeasureTime frame
stages of labor;analgesic consumption;

Countries

China

Contacts

Public Contactjinhua

Yunnan First People's Hospital

Jinhuakm@163.com+86 138 8866 8869

Outcome results

None listed

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