Skip to content

Comparative study on the analgesic effect of liposome bupivacaine vs ropivacaine for popliteal sciatic nerve+saphenous nerve block after tibial and fibular internal fixation surgery

Comparative study on the analgesic effect of liposome bupivacaine vs ropivacaine for popliteal sciatic nerve+saphenous nerve block after tibial and fibular internal fixation surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082797
Enrollment
Unknown
Registered
2024-04-08
Start date
2024-04-08
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

Pain after tibiofibular internal fixation

Interventions

Ropivacaine group:Ultrasound guided saphenous nerve block: 10ml of 0.5% ropivacaine
Popliteal sciatic nerve block under ultrasound: 20ml of 0.5% ropivacaine.
Liposome bupivacaine group:Ultrasound guided saphenous nerve block: 10ml liposomal bupivacaine (89mg, 0.89%)
Ultrasound guided popliteal sciatic nerve block: 20ml (177mg, 0.89%) of liposome bupivacaine.

Sponsors

Zhejiang Xiaoshan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) ASA1-3 level; (2) age =18 years old, =65 years old;

Exclusion criteria

Exclusion criteria: Chronic pain syndrome, long-term use of opioid drugs (over 1 month), body mass index greater than 40kg/m2, allergic to investigational drugs, impaired cognitive function, contraindications to regional anesthesia, severe kidney disease (estimated glomerular filtration rate less than 50ml/min), congestive heart failure grade 3-4, severe liver disease, defined as current or past diagnosis of acute/subacute liver necrosis, acute liver failure, chronic liver disease, liver abscess, liver coma, hepatorenal syndrome, and other liver diseases.

Design outcomes

Primary

MeasureTime frame
Duration of analgesia;

Secondary

MeasureTime frame
Dosage and parameters of sufentanil in analgesia pump 48h after surgery.;NRS pain scores (0-10) at rest and during activity were assessed every 4h for 72 hours after surgery.;Sensorimotor block was scored every 4h for 48h after surgery.;The patient's gender, age y, height cm, weight kg, ASA rating and other basic information were recorded.;Early activity time, hospital discharge date, and satisfaction score were recorded.;Adverse events such as patient falls, neurological damage, surgical infection, or accidental admission to the intensive care unit were recorded.;

Countries

China

Contacts

Public ContactZhong Mei

Zhejiang Xiaoshan Hospital

meizhong@zju.edu.cn+86 189 6997 9723

Outcome results

None listed

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