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Comparison of postoperative analgesia after abdominal surgery using intravenous patient-controlled analgesia device between conventional and optimizing basal infusion mode

Comparison of postoperative analgesia after abdominal surgery using intravenous patient-controlled analgesia device between conventional and optimizing basal infusion mode

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002777
Enrollment
204
Registered
2018-04-05
Start date
2018-09-03
Completion date
Unknown
Last updated
2022-11-28

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

Conditions

None listed

Interventions

Drug, Medical Device : First, all participants will be allocated into one of either traditional basal infusion mode group (group TM) or optimizing basal infusion mode (group OBIM) using random assignm

Sponsors

Chosun University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

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

MeasureTime frame
Numeric Rating Score (NRS)

Secondary

MeasureTime 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

Public ContactSANGHUN KIM

Chosun University Hospital

drshkim4187@yahoo.co.kr+82-62-220-3578

Outcome results

None listed

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