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Analysis of the effects of epidural and intravenous analgesia after caesarean section: an observational retrospective study

Analysis of the effects of epidural and intravenous analgesia after caesarean section: an observational retrospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500106519
Enrollment
Unknown
Registered
2025-07-24
Start date
2025-08-15
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Caesarean section

Interventions

PCEA group:None

Sponsors

Xianya Hospital Central South University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Elective cesarean section, receiving intrathecal anesthesia, postoperative patient-controlled analgesia, postoperative follow-up visits.

Exclusion criteria

Exclusion criteria: Mothers with comorbid obstetric disease; those with complex general anesthesia or nerve block; those with preoperative epidural labor analgesia; those who changed analgesic modalities within 24 hours; those who used PCA for less than 24 hours; those who were admitted to the ICU for various reasons in the postoperative period; and those who had important clinical information about the patient or missing data from the follow-up visits.

Design outcomes

Primary

MeasureTime frame
Incidence of moderate to severe postoperative pain at rest;

Secondary

MeasureTime frame
Pain intensity at rest;Pain intensity during movement;Incidence of moderate to severe postoperative pain during movement;Incidence of dizziness;Severity of nausea;Severity of vomiting;Severity of pruritus;Use of other analgesic drugs;

Countries

China

Contacts

Public ContactZongbin Song

Xianya Hospital Central South University

songzb2001@163.com+86 137 8724 6060

Outcome results

None listed

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