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The effect of DPE technique on the comsuption of epidural ropivacaine for epidural labor analgesia

The effect of DPE technique on the comsuption of epidural ropivacaine for epidural labor analgesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062349
Enrollment
Unknown
Registered
2022-08-02
Start date
2022-08-05
Completion date
Unknown
Last updated
2023-12-19

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 combined with epidural technique
EP group :Epidural technique

Sponsors

Women and Children's Hospital Affiliated to Jiaxing University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Primiparous, singleton pregnancy. 2. Gestation 37-42 weeks, age 20-40 years. 3. American Society of Anesthesiologists physical status II parturients. 4. Cervical dilation 2-5 cm. 5. Numeric rating scale (NRS)pain score = 5 (scale: 0= no pain, 10= worst pain imaginable). 6. Requesting neuraxial labor analgesia.

Exclusion criteria

Exclusion criteria: 1. Body mass index (BMI) > 40 kg/m2. 2. Any contraindications to neuraxial analgesia. 3. Administration of opioid or sedative drug within 4 hours before requesting neuraxial analgesia. 4. Allergy to ropivacaine or sufentanil. 5. Known fetal anomaly.

Design outcomes

Primary

MeasureTime frame
Consumption of ropivacaine per hour;—

Secondary

MeasureTime frame
PCEA press number;delivery mode;Maternal satisfaction;neonatal weight;Apgar scare;PH value of neonatal blood gas;lactic acid;—

Countries

China

Contacts

Public ContactXiao Fei

Women and Children's Hospital Affiliated to Jiaxing University

yhq20113956@163.com+86 137 0659 7501

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026