Evaluation of dosage in Intravenous Patient-Controlled Analgesia for Post-Cesarean Section Pain Managem

Effects of continuous infusion of intravenous patient-controlled analgesia in postoperative pain management of elective cesarean section: a pilot study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0008769

Enrollment

Registered

2023-09-07

Start date

2022-11-18

Completion date

Unknown

Last updated

2023-09-18

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

Conditions

None listed

Interventions

Drug : The administration protocol for IVA was as follows: - Prepare a mixture of fentanyl 2250 mcg, nefopam 60 mg, paracetamol 3 g, and ramocetron 0.6 mg in 150 ml of normal saline solution. - Set t

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Patient scheduled for elective cesarean section and prescribed intravenous patient-controlled analgesia

Exclusion criteria

Exclusion criteria: Patients with a history of allergies to opioids, non-opioid analgesics and local anesthetics, drug abuse, without continuous would infusion catheter, and undergoing emergency CS

Design outcomes

Primary

Measure	Time frame
Opioid consumption and VAS score	—

Secondary

Measure	Time frame
opioid induced side effects;need for rescue analgecis	—

Countries

Korea, Republic of

Contacts

Public ContactJeong Yeon Kim

Samsung Changwon Medical Center

gojy87@naver.com+82-55-233-6048

Outcome results