Effects of regimen change in postoperative pain management of elective cesarean sectio
Not Applicable
Recruiting
- Conditions
- Pregnancy, childbirth and the puerperium
- Registration Number
- KCT0007610
- Lead Sponsor
- Samsung Changwon Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 600
Inclusion Criteria
Patients who underwent elective Cesarean section from January 2019 to August 2021 and were prescribed intravenous patient-controlled analgesia.
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
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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.