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Effect of transversus abdominis plane block combined with rectus sheath block on early postoperative pain and quality of recovery in kidney transplant patients

Effect of transversus abdominis plane block combined with rectus sheath block on early postoperative pain and quality of recovery in kidney transplant patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096785
Enrollment
Unknown
Registered
2025-02-06
Start date
2025-02-08
Completion date
Unknown
Last updated
2025-02-10

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

Conditions

End-Stage Kidney Disease

Interventions

Test Group (Group R):0.33% ropivacaine 30ml [surgical incision lateral transversus abdominis plane (TAP) block 20ml combined with rectus sheath block (RSB) 10ml]
Control group (Group NS):normal saline 30 ml

Sponsors

Second Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients clinically diagnosed with end-stage kidney disease who are scheduled to undergo kidney transplantation in the near future; 2. aged between 18 and 65 years; 3. with a BMI of 18-30 kg/m²; 4. classified as ASA III to IV; 5. able to communicate effectively and cooperate in completing pain assessment scales and follow-up evaluations; 6. who voluntarily agree to participate and sign an informed consent form after a thorough explanation of the clinical trial content.

Exclusion criteria

Exclusion criteria: 1. Patients who have previously undergone kidney transplantation; 2. those with severe cardiovascular, hepatic, neurological, or pulmonary diseases that prevent them from tolerating general anesthesia; 3. individuals who are allergic to the anesthetic drugs used in the study; 4. patients with psychiatric or neurological disorders that hinder their ability to complete pain assessments and follow-up evaluations; 5. those who have recently used analgesic medications or are undergoing long-term treatment with psychotropic drugs; 6. individuals with alcohol dependence or opioid abuse; 7. patients with contraindications for abdominal wall nerve blocks, such as coagulopathy, infection at the puncture site, or tumors.

Design outcomes

Primary

MeasureTime frame
completely painless time after waking up;restlessness score during wakefulness;visual analogue scale;

Secondary

MeasureTime frame
heart rate;mean arterial pressure;15-item quality of recovery scale;Information related to surgery and anesthesia;Postoperative follow-up situation;Adverse reaction monitoring;liver and kidney function;

Countries

China

Contacts

Public ContactChen Qi

Second Affiliated Hospital of Anhui Medical University

cq_911@126.com+86 138 6610 3453

Outcome results

None listed

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