None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: A. Patients scheduled to undergo surgery of the abdomen B. American Society of Anesthesiologists (ASA) Physical Status classification I, II, III C. Adult between 20 and 70 years D. Patients who want the postoperative pain control E. Patients who have agreed to voluntarily participate in this clinical study
Exclusion criteria
Exclusion criteria: A. Patients with neuromuscular disorders, above moderate hepatic and renal dysfunction, thyroid functional abnormality B. Patients with severe respiratory suppression C. Patients with allergies of medicines using study D. Patients who are unable to understand how the use of PCA device E. Patients who are hard to describe the degree of pain F. Patients who are unable to listen, read and understand Korean (Including foreigners) G. The vulnerable environment participants (pregnant women, patients who are breastfeeding, etc.)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Numeric Rating Score (NRS) | — |
Secondary
| Measure | Time frame |
|---|---|
| Presence and its cause of stop of patient-controlled analgesia device;accumulative amount of infused medicine through patient-controlled analgesia device;Type and dose of additional analgesic;Type and dose of antiemtics | — |
Countries
Korea, Republic of
Contacts
Chosun University Hospital