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Ultrasound-guided transversalis fascia block via the superior lumbar triangle for postoperative analgesia in laparoscopic nephrectomy: a prospective study

Ultrasound-guided transversalis fascia block via the superior lumbar triangle for postoperative analgesia in laparoscopic nephrectomy: a prospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113989
Enrollment
Unknown
Registered
2025-12-05
Start date
2025-12-05
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

postoperative pain

Interventions

Test group:ultrasound-guided transversalis fascia block via the superior lumbar triangle

Sponsors

Beijing Friendship Hospital of Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Scheduled for elective laparoscopy nephrectomy under general anesthesia ; (2) American Society of Anesthesiologists (ASA) physical status class I–III; (3) Age 18–70 years; (4) Body mass index (BMI) < 30 kg/m²; (5) Voluntarily agree to use sufentanil for patient-controlled intravenous analgesia (PCIA) for 24–48 hours; (6) Voluntarily accept the anesthesia protocol and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Contraindications to regional anesthesia (coagulation dysfunction, local infection); (2) Allergy to local anesthetics; (3) Anatomical barriers to regional anesthesia; (4) Severe comorbidities involving vital organs (heart, lung, brain, kidney) or severe systemic diseases; (5) History of chronic pain requiring long-term use of analgesic or sedative medications; (6) Psychiatric disorders or cognitive impairment hindering effective communication.

Design outcomes

Primary

MeasureTime frame
cumulative intravenous morphine equivalent consumption at 24 h;

Secondary

MeasureTime frame
dermatomal coverage of sensory block;blood pressure and heart rate following block;NRS pain scores at 1, 6, 24, and 48 hours postoperatively (both at rest and after activity);time to first patient-controlled analgesia (PCA) demand;rescue analgesia requirement;Quadriceps femoris strength;the incidence of side effects;

Countries

China

Contacts

Public ContactHao Dandan

Beijing Friendship Hospital of Capital Medical University

hdd_anesthesia@163.com+86 151 2002 2447

Outcome results

None listed

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