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Application Study of Bupivacaine Liposome in Postoperative Analgesia and Therapeutic Efficacy Following Elbow Arthrolysis

Application Study of Bupivacaine Liposome in Postoperative Analgesia and Therapeutic Efficacy Following Elbow Arthrolysis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103911
Enrollment
Unknown
Registered
2025-06-09
Start date
2025-06-09
Completion date
Unknown
Last updated
2025-06-16

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

Conditions

Post-traumatic Stiffness of the Elbow

Interventions

liposomal bupivacaine group: Liposomal bupivacaine group will receive 10 ml of liposomal bupivacaine mixed with 10 ml of 0.5% ropivacaine as a loading dose, followed by connection to an electronic ana
Control group:Control group will receive 20 ml of 0.5% ropivacaine as a loading dose, followed by connection to an electronic analgesic pump delivering 200 ml of 0.2% ropivacaine, with 10 ml administe

Sponsors

Beijing Jishuitan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. ASA I–III, aged 18–65 years. 2. Diagnosed with posttraumatic elbow stiffness23 and scheduled for open elbow release surgery. 3. Normal coagulation function and no neurological impairment. 4. No infection at the puncture site. 5. Willing to participate and provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. Severe cardiovascular or cerebrovascular diseases and diabetes with peripheral neuropathy. 2. Severe cognitive impairment, hearing loss, or communication difficulties. 3. Hepatic/renal insufficiency, immune or haematological diseases. 4. Malignancy. 5. Postoperative transfer to ICU. 6. Unplanned discharge or refusal to participate. 7. Pathological fractures. 8. History of local anaesthetic allergy. 9. Pregnancy.

Design outcomes

Primary

MeasureTime frame
The weighted area under the curve (AUC) of the average NRS pain score (0–10, where 0 is no pain and 10 is the worst pain) during functional exercises ;

Secondary

MeasureTime frame
NRS pain scores at rest, along with the number of analgesic pump presses, rescue analgesia requests, and the type of rescue analgesia ; Pittsburg sleep quality index(PSQI) ;The range of motion (ROM) improvement;Postoperative recovery quality ;NRS score;Grip strength scores ;Quick-DASH scores;

Countries

China

Contacts

Public ContactLuo Taijun

Beijing Jishuitan Hospital, Capital Medical University

dr_luo@yeah.net+86 189 1012 2356

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 21, 2026