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Ultrasound-guided erector spinae plane block for perioperative analgesia in patients undergoing laparoscopic nephrectomies surgery: A Randomized Controlled Trial

Ultrasound-guided erector spinae plane block for perioperative analgesia in patients undergoing laparoscopic nephrectomies surgery: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068578
Enrollment
Unknown
Registered
2023-02-23
Start date
2023-02-23
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Kidney neoplasms

Interventions

ESPB group:Ultrasound-guided erector spinae plane block with local anesthetics (0.7%ropivacaine 10 ml + 1% lidocaine 10 ml) + 5 mg dexamethasone + 0.5 ug/kg dexmedetomidine
Control group:ultrasound-guided erector spinae plane block with 0.9% saline 20 ml

Sponsors

Department of Anesthesiology, Second Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Patients aged 18-65 years scheduled for elective laparoscopic nephrectomy; 2) ASA I-III; 3) Willing to participate in this study and signed informed consent.

Exclusion criteria

Exclusion criteria: 1) allergy to local anesthetics; 2) BMI > 35 kg/m2; 3) history of mental illness or taking psychotropic drugs; 4) combined with spinal deformity; 5) long-term use of analgesics or sedatives; 6) history of drug abuse, alcohol or opioid abuse; 7) chronic pain or recent acute pain; 8) severe liver and kidney dysfunction; 9) any reason can not cooperate with the study or researchers think it is not suitable for inclusion in this trial

Design outcomes

Primary

MeasureTime frame
the total use of sufentanil during intraoperative period;

Secondary

MeasureTime frame
intraoperative remifentanil consumption;VAS pain scores at rest and coughing at 1 hour, 6 hours, 12 hours, 24 hours, 48 hours after surgery;incidence of nausea and vomiting in the first 24 hour after surgery;times of rescue analgesic;

Countries

China

Contacts

Public ContactMing Yang

Department of Anesthesiology, Second Affiliated Hospital of Army Medical University

1310466364@qq.com+86 18428388228

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026