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Determination of the optimal programmed intermittent epidural bolus volume

Determination of the optimal programmed intermittent epidural bolus volume of 0.1% ropivacaine with 0.5ug/ml sufentanil at labor analgesia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000040917
Enrollment
Unknown
Registered
2020-12-15
Start date
2021-01-01
Completion date
Unknown
Last updated
2021-04-12

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

Conditions

maternal

Interventions

1:PIEB

Sponsors

Ya'an People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 38 Years

Inclusion criteria

Inclusion criteria: (1) request for epidural analgesia; (2) ASA I-II ; (3) Gestational week 37 42 weeks; (4) No pregnancy complications or complications; (5) No previous history of uterine surgery.

Exclusion criteria

Exclusion criteria: (1) The patient refuses; (2) Contraindications to intraspinal anesthesia; (3) Allergy to ropivacaine and sufentanil; (4) Unable to cooperate.

Design outcomes

Primary

MeasureTime frame
VAS;—

Countries

China

Contacts

Public ContactHe Peng

Ya'an People's Hospital

2633797485@qq.com+86 18283560691

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 14, 2026