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Ananlysis of Effectiveness of Liposome Bupivacaine in Reducing Pain After Total Knee Arthroplasty

Ananlysis of Effectiveness of Liposome Bupivacaine in Reducing Pain After Total Knee Arthroplasty

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074631
Enrollment
Unknown
Registered
2023-08-11
Start date
2023-08-01
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Knee arthritis disease

Interventions

Experimental Group:Local injection of liposome bupivacaine 266mg
Control group:Local injection of bupivacaine 150mg+ dexamethasone 5mg

Sponsors

Municipal Hospital of Heze
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: A total of 72 patients with knee osteoarthritis who received TKA under general anesthesia in our hospital from August 2023 to January 2024 were selected. ASA Level I or II. Selection criteria: (1) Age 50-80 years old; (2) The weight is 54 ~ 80kg.

Exclusion criteria

Exclusion criteria: Exclusion criteria: (1) poor compliance; (2) Allergy to the drugs in this study; (3) Daily intake of steroids or strong opioids (morphine, oxycodone, methadone, fentanyl, or ketomidone); (4) alcohol or drug abuse; (5) Rheumatoid arthritis.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale (VAS) score and Ramsay sedation score were performed at 6h, 12h and 24h after surgery;The number of opiates the patient used post-operatively, and the actual number of PCIA compressions;

Secondary

MeasureTime frame
Patient's knee bend angle and first time of getting out of bed;The incidence of adverse reactions and postoperative satisfaction were compared between the two groups;

Countries

China

Contacts

Public ContactLijun Qi

Municipal Hospital of Heze

lijun0108@126.com+86 134 0530 0910

Outcome results

None listed

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