Skip to content

Effect of oliceridine for patient-controlled intravenous analgesia in patients after total knee arthroplasty

Effect of oliceridine for patient-controlled intravenous analgesia in patients after total knee arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105848
Enrollment
Unknown
Registered
2025-07-14
Start date
2025-07-14
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

End-stage osteoarthritis of the knee, Rheumatoid arthritis

Interventions

Sufentanil Group:Tolthetron 4 mg sufentanil 2ug/kg diluted to 100ml with normal saline. The parameters are set to the background infusion speed of 2ml/h, the single compression dose is 0.5ml, the lock
Oliceridine Group:Tropisetron 4 mg Oselidine 0.4 mg/kg diluted to 100 ml with normal saline. The parameters are set to the background infusion speed of 2ml/h, the single compression dose is 0.5ml, the

Sponsors

The Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Aged 65-80 years 2.ASA physical status classification I-III 3.Scheduled for elective total knee arthroplasty under general anesthesia 4.Postoperative patient-controlled intravenous analgesia (PCIA) planned 5.Body mass index (BMI) 18-28 kg/m^2

Exclusion criteria

Exclusion criteria: 1.Presence of significant underlying diseases (e.g., cardio/cerebrovascular, respiratory, hepatic, or renal dysfunction) 2.Inability to complete pain scale assessments due to visual/auditory impairment or illiteracy 3.Pre-existing psychiatric disorders or chronic psychotropic medication use 4.Dependence on opioids or other analgesic medications 5.Contraindications to oliceridine administration

Design outcomes

Primary

MeasureTime frame
Static and dynamic pain visual analogue (VAS) scores;

Secondary

MeasureTime frame
Ramsay Sedation Score;Time to first PCA demand;The total number of PCA compressions within 48 hours;Delivered PCA boluses within 48 hours;Rescue analgesia consumption;QoR-15 scores;Athens Insomnia Scale (AIS) Score;Occurrence of adverse events within 48 hours after surgery;Patient satisfaction;The length of time from the end of the operation to the discharge from the hospital;

Countries

China

Contacts

Public ContactDunyi Qi

The Affiliated Hospital of Xuzhou Medical University

qdy6808@163.com+86 151 6215 9886

Outcome results

None listed

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