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Effect of liposomal bupivacaine in the parasacral ischial plane on analgesia after total knee arthroplasty: a single-center, double-blind, randomized controlled study

Effect of liposomal bupivacaine in the parasacral ischial plane on analgesia after total knee arthroplasty: a single-center, double-blind, randomized controlled study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079606
Enrollment
Unknown
Registered
2024-01-08
Start date
2024-01-30
Completion date
Unknown
Last updated
2024-01-28

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

Conditions

Knee joint disease

Interventions

group I:the parasacral ischial plane was injected with 133mg liposomal bupivacaine
group ?:the parasacral ischial plane was injected with 266mg liposomal bupivacaine

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Requires unilateral total knee arthroplasty; 2.Age 18-80 years; 3.ASA I-II grade; 4.BMI 18-30 kg/m2; 5.Voluntary and signed informed consent form; 6.Ability to walk independently for at least 20 meters; 7.Normal sensory function in the distribution area of the sciatic nerve.

Exclusion criteria

Exclusion criteria: 1.Patients with chronic pain; 2.Preoperative opioid therapy; 3.Allergic to the study drug; 4.Unable to use or understand patient-controlled analgesia (PCA) device; 5.Infection at the site of nerve block puncture; 6.Ultrasound could not identify the anatomical structure or identify the body surface location; 7.Nerve disorders; 8.Coagulation dysfunction; 9.Those who refuse to sign informed consent.

Design outcomes

Primary

MeasureTime frame
Pain score;Blocking onset time;Duration of sensory block;Duration of motor block;Consumption of opioid medications;Rescue analgesia time and frequency;Satisfaction with pain management;

Secondary

MeasureTime frame
Duration of block procedure;Perioperative vital signs;Adverse reactions;Sedation score;Duration of hospitalization;

Countries

China

Contacts

Public ContactZheng Ting

Department of Anesthesiology, Fujian Provincial Hospital

zhengting1223@163.com+86 156 5911 5373

Outcome results

None listed

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