Intravenous patient controlled analgesia of nefopam

Postoperative intravenous patient controlled analgesic efficacy of nefopam after laparoscopic gynecologic surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0001202

Enrollment

Registered

2014-08-19

Start date

2014-03-06

Completion date

Unknown

Last updated

2019-03-11

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

Conditions

None listed

Interventions

Drug : 60 patients scheduled to undergo laparoscopic gynecologic surgery received IV-PCA for postoperative analgesia. Group A (n =30) and B (n = 30) received IV-PCA using combination with morphine 60m

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: American Society of Anesthesiologist (ASA) physical status I–II patients scheduled to undergo laparoscopic gynecologic surgery

Exclusion criteria

Exclusion criteria: Patients with preexisting neurological deficit, renal and hepatic dysfunction, obese (BMI > 30 kg/m2), drug abuse or hypersensitivity to drugs, pregnancy

Design outcomes

Primary

Measure	Time frame
Visual analogue scale (VAS)	—

Secondary

Measure	Time frame
Postoperative nausea and vomiting;Patient satisfaction to postoperative pain control;Rate of patients taking additional opioids requirements ;incidence rate of side effects	—

Countries

Korea, Republic of

Contacts

Public ContactGyeong-Jo Byeon

Pusan National University Yangsan Hospital

byeongj@pusan.ac.kr+82-55-360-2758

Outcome results