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Clinical efficacy of programmed intermittent epidural bolus and patient-controlled epidural infusion for labor analgesia

Clinical efficacy of programmed intermittent epidural bolus and patient-controlled epidural infusion for labor analgesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021142
Enrollment
Unknown
Registered
2019-01-30
Start date
2019-03-01
Completion date
Unknown
Last updated
2019-02-04

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

Conditions

labor analgesia

Interventions

IEB+PCA:intermittent epidural bolus & patient-controlled epidural analgesia
PCA:patient-controlled epidural analgesia

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: gestational weeks more than 37 weeks; head presentation; American Society of Anesthesiologists II; enter the labor; parturient requires labor analgesia;

Exclusion criteria

Exclusion criteria: parturient refuses to join the research; contraindication of epidural puncture; high risk pregnancy; fetal abnormality

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale/Score (VAS);—

Secondary

MeasureTime frame
delivery mode;—

Countries

China

Contacts

Public ContactHaiyang Yu

Peking University First Hospital

yuhaiyang19840123@163.com+86 18600232417

Outcome results

None listed

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