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Effect of epidural labour analgesia infusion regimen on maternal and neonatal outcomes

Effect of epidural labour analgesia infusion regimen on maternal and neonatal outcomes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081994
Enrollment
Unknown
Registered
2024-03-18
Start date
2024-03-25
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

Epidural labour analgesia

Interventions

The experimental group S:Open vein, no fluids
The experimental group L:Infusion rate of 10mL/kg/h
The experimental group H:Infusion rate of 20mL/kg/h

Sponsors

Hangzhou maternity hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Single pregnancy primigravida. 2. 37-41 weeks of gestation. 3. PP <45 mm Hg. 4. ASA class II.

Exclusion criteria

Exclusion criteria: 1. Age 30kg/m2. 3. Height <150cm. 4. Contraindication to intralesional anaesthesia. 5. Systolic blood pressure less than 90 mmHg. 6. Fetal intrauterine growth restriction or chromosomal abnormalities, category 2 or 3 FHR.

Design outcomes

Primary

MeasureTime frame
blood pressure;variation in fetal heart rate;—

Countries

China

Contacts

Public ContactBing Hu

Hangzhou maternity hospital

hubing0206105@126.com+86 135 8768 5029

Outcome results

None listed

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