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Effect of low thoracic paravertebral block via the arcuate ligament under direct visualization on the quality of postoperative recovery after laparoscopic donor nephrectomy for living kidney transplantation

Effect of low thoracic paravertebral block via the arcuate ligament under direct visualization on the quality of postoperative recovery after laparoscopic donor nephrectomy for living kidney transplantation: a single-center, blind, prospective randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094612
Enrollment
Unknown
Registered
2024-12-25
Start date
2024-12-31
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

None listed

Interventions

Experimental group:Low thoracic paravertebral block via the arcuate ligament under direct visualization
Control group:Ultrasound-guided transverse abdominal muscle block

Sponsors

Beijing Friendship Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. There is no restriction on gender, age18-70 years, ASA grade I~II; 2. Patients scheduled to undergo laparoscopic donor nephrectomy.

Exclusion criteria

Exclusion criteria: 1. Use of anticoagulant drugs before surgery; 2. Patients with a history of long-term opioid addiction or use of any analgesic medication for more than 3 months; 3. Patients who are allergic to the drugs used in standardized anesthesia; 4. Severe cardiac, cerebrovascular and hematological diseases; 5. History of drug or alcohol abuse; 6. Those who have undergone thoracic or spinal surgery and spinal deformity; 7. Those who have insufficient understanding of QOR-15 score before surgery; 8. Local infection or systemic infection at the puncture site; 9. Refusal to participate in the observer.

Design outcomes

Primary

MeasureTime frame
Quality of postoperative recovery within 24 hours post-operatively;

Secondary

MeasureTime frame
NRS scores;AFPS scores;Time to first opioid use;The cumulative opioid consumption post-operatively;Quality of postoperative recovery;Exhaust time;Ambulation time;Sleep in-terruptions as a result of pain;Hospital stay;Time to remove urinary catheters and drains;Patient satisfaction;Hemodynamic Indicators;Use of rescue analgesics;

Countries

China

Contacts

Public ContactLingli Cui

Beijing Friendship Hospital, Capital Medical University

clinly@126.com+86 10 6313 8761

Outcome results

None listed

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