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A prospective study on satisfaction and influencing factors of labor analgesia

A prospective study on satisfaction and influencing factors of labor analgesia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500115584
Enrollment
Unknown
Registered
2025-12-29
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Labor analgesia

Interventions

Observation group:None

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: (1) Gestational age >=37 weeks, cephalic presentation when applying for labor analgesia; (2) patients voluntarily requested and accepted intraspinal labor analgesia; (3) Sufficient cognitive and communication skills to cooperate with prenatal data collection, delivery data recording and postpartum satisfaction assessment; (4) Informed consent was signed.

Exclusion criteria

Exclusion criteria: (1) There were contraindications to spinal anesthesia (such as coagulopathy, infection at the puncture site, severe spinal deformity, etc.); (2) History of mental illness, cognitive dysfunction or language communication disorder, unable to complete the questionnaire; (3) Prenatally diagnosed depression or anxiety disorder (through medical records) or EPDS>=10 at enrollment; (4) Incomplete clinical data or withdrawal from the study.

Design outcomes

Primary

MeasureTime frame
Satisfaction;

Countries

China

Contacts

Public ContactLiu Huili

Peking University Third Hospital

dr_zeng@sina.com+86 10 8226 7272

Outcome results

None listed

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