Effect of intraoperative low-dose naloxone infusion on postoperative pain control

Effect of intraoperative low-dose naloxone infusion on postoperative pain control: randomized double-blinded controlled trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0000515

Enrollment

Registered

2012-08-31

Start date

2012-08-22

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 : Patients in naloxone group receives naloxone 0.1 mcg/kg/hr, and patients in control group receives same amount of saline.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. elective living-donor hepatectomy 2. who consented present study 3. over 20 yr old

Exclusion criteria

Exclusion criteria: 1. alleric history to naloxone 2. postoperative intubating state 3. sedated patient 4. cannot verbal communication 5. do denied to participate

Design outcomes

Primary

Measure	Time frame
Visual Analogue Pain Scale;fentanyl requirement	—

Secondary

Measure	Time frame
rescue analgesic requirement;blood pressure; heart rate	—

Countries

Korea, Republic of

Contacts

Public ContactSung-Hoon Kim

Asan Medical Center

Outcome results