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Comparison of preincisional vs postincisional administration of nefopam on postoperative analgesic requirement and recovery of pulmonary function

Effects of preincisional administration of nefopam on postoperative analgesic requirement and recovery of pulmonary function

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002559
Enrollment
150
Registered
2017-11-24
Start date
2013-03-04
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, Others(Pre-incisional administration vs post-incisional adminidtration) : Group 1 (control group): 50 mL saline administration at 30 min before operation and administration of nefopam 20 mg in 5

Sponsors

Chonbuk National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients undergoing laparoscopic colectomy

Exclusion criteria

Exclusion criteria: 1. Patients can not communication 2. Hypersensitivity to nefopam 3. History of previous postoperative nausea and vomiting or motion sickness 4. Severe pulmonary disease 5. Patients do not use postoperative patient-controlled analgesia

Design outcomes

Primary

MeasureTime frame
postoperative analgesic requirement and pain intensity

Secondary

MeasureTime frame
recovery of pulmonary function

Countries

Korea, Republic of

Contacts

Public ContactSeonghoon Ko

Chonbuk National University

shko@jbnu.ac.kr+82-63-250-1979

Outcome results

None listed

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