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Study on local anesthetic dosage in ultrasound-guided anterior lumbar muscle block

Study on local anesthetic dosage in ultrasound-guided anterior lumbar muscle block

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096318
Enrollment
Unknown
Registered
2025-01-21
Start date
2024-05-04
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Abdominal surgery analgesia

Interventions

Ultrasound-guided subcostal anterior lumbar quadratus block group:Ultrasound-guided subcostal anterior lumbar quadratus block in patients undergoing abdominal surgery

Sponsors

Department of Anesthesiology, Affiliated Hospital of Yangzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective abdominal surgery; 2. Male or female, age >= 18 years old; 3. ASA ?-?; 4. BMI 18~35.0 kg/m^2; 5. No psychiatric or neurological disorders; 6. No puncture site infection; 7. Clearly understand, voluntarily participate in the study, and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients who have taken non-steroidal drugs for a long time before surgery or have a history of overdose opioid analgesia; 2. Patients with preoperative hyperthyroidism or hypothyroidism, severe cardiovascular disease, severe anemia, and significant abnormal heart, lung, liver, and kidney functions; 3. Patients with a history of local anesthetic drug allergy; 4. Contraindications or complications of quadratus lumbar block, including coagulation dysfunction or local infection; 5. Have undergone retroperitoneal surgery or spinal deformities, puncture site infections, or anatomical variations; 6. Refused to participate in the trial.

Design outcomes

Primary

MeasureTime frame
Subcostal anterior lumbar quadratus block plane range;

Secondary

MeasureTime frame
Number of times of remedial analgesia (flurbiprofen) administered;Blood pressure and heart rate;Visual Analogue Scale;Nausea, vomiting and other adverse reactions;hospital stay;complications (hematoma, infection, abdominal organ injury, local anesthetic poisoning, etc.);

Countries

China

Contacts

Public ContactZhang Jianyou

Affiliated Hospital of Yangzhou University

1152207357@qq.com+86 138 3581 3811

Outcome results

None listed

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