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Effects of regimen change in postoperative pain management of elective cesarean section

Effects of intravenous patient controlled analgesia regimen change in postoperative pain management of elective cesarean section: A single center retrospective evaluation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0007610
Enrollment
600
Registered
2022-08-05
Start date
2022-07-21
Completion date
Unknown
Last updated
2022-09-20

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

Conditions

None listed

Interventions

None listed

Sponsors

Samsung Changwon Medical Center
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patients who underwent elective Cesarean section from January 2019 to August 2021 and were prescribed intravenous patient-controlled analgesia.

Exclusion criteria

Exclusion criteria: 1. If clinical informations are insufficient in the patient's medical records 2. If the intravenous patient-controlled analgesia infusion device is broken and discarded

Design outcomes

Primary

MeasureTime frame
The primary outcome aims to find out if there is a significant difference in intravenous patient-controlled analgesia discard and additional prescriptions, side effects, and prescription of analgesics in the ward as intravenous patient-controlled analgesia regimen is changed in patients undergoing elective Cesarean section.

Secondary

MeasureTime frame
The secondary outcome aims to find out if there is a significant difference in intravenous patient-controlled analgesia discard and additional prescriptions, side effects, and prescription of analgesics in the ward in patients with wound infiltration with local anesthetics after Cesarean section.

Countries

Korea, Republic of

Contacts

Public ContactJeong won Park

Masan Samsung Medical Center

comengjw@naver.com+82-55-233-5521

Outcome results

None listed

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