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Analgesic effect of bupivacaine liposome in brachial plexus block after forearm fracture

Analgesic effect of bupivacaine liposome in brachial plexus block after forearm fracture

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117124
Enrollment
Unknown
Registered
2026-01-20
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Forearm fracture postoperative pain, postoperative analgesia, chronic pain

Interventions

Bupivacaine liposome group:Axillary nerve block with bupivacaine liposome 133 mg after operation
Ropivacaine group:Axillary nerve block with 0.25 % ropivacaine 10 ml at the end of operation.

Sponsors

Shaanxi 215 Hospital of nuclear industry
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.The age was 18-80 years old. 2.ASA grade I ~ III; 3.Cognitive function is normal, can cooperate with; 4.To be unilateral forearm fracture open reduction and internal fixation; 5.Agree to receive ultrasound-guided brachial plexus block anesthesia; 6.Voluntary participation and signing of informed consent.

Exclusion criteria

Exclusion criteria: 1.Allergic to local anesthetics or research drugs; 2.Puncture site infection; 3.Complicated with severe neurological diseases; 4.Severe liver and kidney dysfunction; 5.Coagulation disorders; 6.History of chronic pain or long-term use of opioids; 7.Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Resting state VAS score at 48 h;

Secondary

MeasureTime frame
The VAS scores at 24h, 48h and 72h after operation were recorded.;The pressing times of analgesia pump and the amount of sufentanil used within 24h, 48h and 72h.;Satisfaction of analgesic effect;The time of first remedial analgesia and the dose of remedial analgesics were recorded.;The degree and duration of motor block at 2 h, 6 h, 12 h, 24 h, 48 h and 72 h after operation were recorded.;Incidence of postoperative adverse reactions;length of hospital stay;The resting state VAS scores at 2 h, 6 h, 12 h, 24 h and 72 h after operation were recorded.;Gastrointestinal peristalsis recovery time;

Countries

China

Contacts

Public ContactDu JianLong

Shaanxi 215 Hospital of Nuclear Industry

sd9bc@163.coom+86 138 9109 5322

Outcome results

None listed

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