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Application of bupivacaine liposomes in thoracolumbar interfascial plane block after lumbar surgery

Application of bupivacaine liposomes in thoracolumbar interfascial plane block after lumbar surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092097
Enrollment
Unknown
Registered
2024-11-08
Start date
2024-11-10
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

lumbar spondylolisthesis Lumbar disc herniation Lumbar vertebral fracture

Interventions

Bupivacaine liposome group (LB group):Received bupivacaine liposomes for TLIP block after surgery
Rawpivacaine group (Group R):Received rawpivacaine for TLIP block after surger

Sponsors

The First Affiliated Hospital of Anhui University of Science and Technology (Huainan First People's Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 64 Years

Inclusion criteria

Inclusion criteria: Age: 20 to 64 years. Physical fitness index (BMI):18.5-28 kg/m2. Patients proposed to undergo elective lumbar surgery, including lumbar discectomy, lumbar fusion, etc. American Association of Anesthesiologists (ASA) grades I-III. There was no preoperative history of severe neuropathic pain. Signed the informed consent form and was willing to undergo the follow-up visit.

Exclusion criteria

Exclusion criteria: Allergic or contraindication to local anesthetic drugs (including bupivacaine, ropivacaine and its derivatives). The coagulation time and platelet number were abnormal. Infection at the puncture site. There are severe cardiovascular, respiratory, liver and kidney dysfunction. Long-term administration of opioids before surgery. Pregnant or lactating women. Mental illness or cognitive impairment, can not cooperate with the researcher to complete the questionnaire survey.

Design outcomes

Primary

MeasureTime frame
QoR-40(Quality of Recovery-40);

Secondary

MeasureTime frame
NRS scores at 6,12,24,48,72 hours;Time of the first compression of the postoperative analgesic pump;Number of additional remedial analgesia required 72 hours after surgery;OBAS(Overall Benefit of Analgesia Score);

Countries

China

Contacts

Public ContactYuanyuan Zhao

The First Affiliated Hospital of Anhui University of Science and Technology (Huainan First People's Hospital)

541289680@qq.com+86 158 5543 2002

Outcome results

None listed

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