None listed
Conditions
Interventions
Drug : During surgery, 40 mg of nefopam is mixed with 100 ml of normal saline and administered intravenously for intervention group.
Sponsors
The Catholic University of Korea, Eunpyeong St. Mary's Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) American Society of Anesthesiologists (ASA) physical status I or II 2) adults between 19 and 75 years of age.
Exclusion criteria
Exclusion criteria: 1) Patients who disagree with the study 2) Patients who have difficulty understanding and agreeing with the explanation of the study due to cognitive impairment. 3) Pregnant women and lactating women 4) American Society of Anesthesiologists (ASA) physical status 3 or higher 5) Age under 19 or over 75 6) a patient with a history of convulsions or convulsions 7) Patients receiving MAO inhibitors and anti-cholinergic drugs 8) Patients with urethral and prostate disorders 9) Patients with closed-angle glaucoma (increased intraocular pressure)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| RUQ pain(Visceral pain) | — |
Secondary
| Measure | Time frame |
|---|---|
| Umbilicus pain(Somatic pain), Shoulder pain(Referred pain);Patients' satisfaction(QoR 15 questionnaire) | — |
Countries
Korea, Republic of
Contacts
Public ContactSoyeon Lee
The Catholic University of Korea, Eunpyeong St. Mary's Hospital
Outcome results
None listed