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Comparison of painless delivery time and analgesic effect in different populations

Comparison of painless delivery time and analgesic effect in different populations

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200062630
Enrollment
Unknown
Registered
2022-08-14
Start date
2022-08-16
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

Painless delivery

Interventions

case series:None

Sponsors

Karamay People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: All natural parturients from 2022 to 2024.

Exclusion criteria

Exclusion criteria: Contraindications of spinal anesthesia, emergency status, insufficient delivery conditions of pregnant women, macrosomia, etc.

Design outcomes

Primary

MeasureTime frame
Cervical opening for the first application for spinal anesthesia;Visual Analogue Scale scores;—

Secondary

MeasureTime frame
Time of first active pressing patient controlled analgesia;dosage of patient controlled analgesia;—

Countries

China

Contacts

Public ContactDeng Xiaoqian

Karamay People's Hospita

50058837@qq.com+86 13880408185

Outcome results

None listed

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