Skip to content

Study on Ultrasound-Guided Quadratus Lumborum Block at the Lateral Supra-Arcuate Ligament for Postoperative Analgesia in Laparoscopic Inguinal Hernia Repair

Study on Ultrasound-Guided Quadratus Lumborum Block at the Lateral Supra-Arcuate Ligament for Postoperative Analgesia in Laparoscopic Inguinal Hernia Repair

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102330
Enrollment
Unknown
Registered
2025-05-13
Start date
2024-09-26
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Inguinal hernia

Interventions

Lateral arcuate ligament approach of quadratus lumborum block group: Prior to anesthesia induction, patients will receive an ultrasound-guided quadratus lumborum block at the lateral arcuate ligament
Transversus abdominis plane block group:Prior to anesthesia induction, patients will receive an ultrasound-guided transversus abdominis plane block. Twenty milliliters of 0.5% ropivacaine will be adm
Anterior approach quadratus lumborum block group:Prior to anesthesia induction, patients will receive an ultrasound-guided anterior quadratus lumborum block . Twenty milliliters of 0.5% ropivacaine wi

Sponsors

The First Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Male patients aged 18-65 years scheduled for unilateral laparoscopic inguinal hernia repair 2. ASA physical status I-III with satisfactory cardiopulmonary function to tolerate general anesthesia (e.g., hypertensive patients with well-controlled blood pressure on regular medication and without significant target organ damage)

Exclusion criteria

Exclusion criteria: 1. Severe organ dysfunction or coagulation disorders 2. Diabetes mellitus 3. History of chronic pain 4. Analgesic drug abuse or addiction (including opioids) 5. Infection at the injection site 6. History of local anesthetic allergy or contraindications 7. Anatomical alterations blocking local anesthetic spread 8. Inability to communicate effectively

Design outcomes

Primary

MeasureTime frame
Total cumulative morphine equivalent consumption at 24 hours postoperatively;

Secondary

MeasureTime frame
Sensory block level;Intraoperative consumption of sufentanil and remifentanil;postoperative rescue analgesic consumption and PCA attempts within 48 hours;Numerical Rating Scale (NRS) pain scores at 2, 4, 6, 12, 24, and 48 hours postoperatively;Time to first PCIA request;Time to first rescue analgesia; Time to first ambulation and flatus;Quality of Recovery-15 (QoR-15) scores at 24 and 48 hours postoperatively;Analgesic satisfaction score before discharge;Perioperative MAP and HR measurements were obtained at: OR admission , 2h , 4h , 6h , 12h , 24h , and 48h after surgery;

Countries

China

Contacts

Public ContactLiu Tianyin

The First Affiliated Hospital of Nanchang University

34700117@qq.com+86 135 7607 5317

Outcome results

None listed

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