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Efficacy and Safety of repeated administration of intravenous acetaminophen injection for pain management after total knee arthroplasty

Efficacy and Safety of repeated administration of intravenous acetaminophen injection for pain management after total knee arthroplasty - Efficacy of intravenous acetaminophen injection for pain management after TKA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000031692
Enrollment
60
Registered
2018-03-12
Start date
2018-03-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

knee osteoarthritis rheumatoid arthritis

Interventions

Study group:Fentanyl sustained intravenous administration given after operation end. And use the Intravenous acetaminophen 4 times per 6 hour.Dosage is 15 mg/kg for the patient less than 50 kg in weig

Sponsors

Yamaguchi University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Subjects eligible for inclusion in this study have to fulfill all of following criteria and be judged eligible for the study by the investigator. 1) Those who have ability to provide written consent to participate in the study. 2)Patients of American Society of Anesthesiologists (ASA) physical status classification 1 and 2 and 3. 3)Patients aged 20 years or older at the time of obtaining informed consent.

Exclusion criteria

Exclusion criteria: 1)Aspirin-induced asthma or a history of diseases of aspirin-induced asthma. 2)Any subject with a past history of anaphylaxis due to acetaminophen. Any subject with blood abnormality, hepatopathy, kidney damage or cardiac dysfunction. 3)patients with liver failure. 4)Patients with NSAIDS contraindications 5)Women who are pregnant, maybe pregnant or lactation. 6)Any subject with blood abnormality, hepatopathy, kidney damage or cardiac dysfunction. 7)Any condition that, in the opinion of the investigator, would make the patient unsuitable for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
Pain intensity at rest is measured with NRS for 24 hours after surgery.

Countries

Japan

Contacts

Public ContactKazushige Seki

Yamaguchi University Graduate School of Medicine Department of Orthopedic Surgery

sk0105@yamaguchi-u.ac.jp0836-22-2268

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026