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The Efficacy of Programmed Intermittent Epidural Bolus Compared with Continuous Epidural Infusions for Postcesarean Delivery Analgesia: A randomized controlled trial

The Efficacy of Programmed Intermittent Epidural Bolus Compared with Continuous Epidural Infusions for Postcesarean Delivery Analgesia: A randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021499
Enrollment
Unknown
Registered
2019-02-24
Start date
2019-03-01
Completion date
Unknown
Last updated
2019-02-25

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

Conditions

Postoperative Pain

Interventions

A: programmed intermittent epidural bolus
B: continuous epidural infusion

Sponsors

Women's Hospital, School of Medicine Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Healthy,full-term women with singleton pregnancy scheduled cesarean delivery under neuraxial anesthesia; 2. Submitted permission for postoperative epidural analgesia.

Exclusion criteria

Exclusion criteria: 1. History of andominal surgery(except cesarean delivery); 2. History of intra-abdominal infection; 3. Congenital uterine malformation.

Design outcomes

Primary

MeasureTime frame
postoperative pain score;—

Secondary

MeasureTime frame
the total dose of ropivacain 48 hours after surgery;—

Countries

China

Contacts

Public ContactChen Xinzhong

Women's Hospital, School of Medicine Zhejiang University

chenxinz@zju.edu.cn+86 0571 87061501

Outcome results

None listed

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