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Effect of liposomal periarticular injection of bupivacaine on postoperative analgesia and early exercise in patients with unicompartmental knee arthroplasty: a prospective, randomized controlled clinical study

Effect of liposomal periarticular injection of bupivacaine on postoperative analgesia and early exercise in patients with unicompartmental knee arthroplasty: a prospective, randomized controlled clinical study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088414
Enrollment
Unknown
Registered
2024-08-19
Start date
2024-09-01
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Pain

Interventions

Bupivacaine liposome group(PAI-L):Periarticular injection with the regimen "Bupivacaine liposome 266 mg + saline, total volume 50 ml".
Ropivacaine group (PAI-R):Periarticular injection with the regimen "Ropivacaine 150mg + Morphine 10mg + Methylprednisolone 40mg + Saline, total volume 50ml".

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Patients undergoing unilateral UKA for the first time; 2) Aged 18 years or older; 3) ASA class I-III; 4) Informed about the clinical trial and signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1) Pregnant patients; 2) History of allergy to amide-type local anaesthetics, or allergy to liposomal bupivacaine; 3) Combination of severe hepatic, renal, and cardiac insufficiency; 4) Combination of comorbidities that may affect postoperative recovery, such as sequelae of cerebral infarction, Parkinson's disease, and Alzheimer's disease, etc. 5) Previous history of narcotic dependence and drug abuse; 6) Combination of psychiatric disorders; 7) Currently on hormone use; 8) Preoperative electrocardiograms suggesting that the heart rate is <50 beats, or there is a prolonged QT interval, or pre-excitation syndrome.

Design outcomes

Primary

MeasureTime frame
Pain;

Secondary

MeasureTime frame
knee mobility;Time to first active straight leg raise, time to get out of bed;Patient satisfaction;Dosage of postoperative analgesic drugs;

Countries

China

Contacts

Public ContactChen Feng

Shanghai General Hospital

smmuchenfeng@163.com+86 135 4679 1339

Outcome results

None listed

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