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Effects of ultrasound-guided erector spinae plane block on perioperative pain control and short-term outcome in lumbar laminoplasty

Effects of ultrasound-guided erector spinae plane block on perioperative pain control and short-term outcome in lumbar laminoplasty

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026706
Enrollment
Unknown
Registered
2019-10-19
Start date
2018-09-01
Completion date
Unknown
Last updated
2019-11-11

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

Conditions

lumbar spinal canal stenosis

Interventions

Control group:Patient-controlled intravenous analgesia
Experimental group:Ultrasound-guided erector spinae plane block with patient-controlled intravenous analgesia

Sponsors

Department of Anesthesiology, the Second Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: This study was approved by the Research Ethics Committee of the Second Hospital of Shandong University, all Patients or authorized family members have signed informed consent. Seventy patients undergoing lumbar laminoplasty, aged more than 18 years old, body mass index between 18 and 35, ASA I-III, agreed to accept one of the two analgesic regimens randomly, were divided into two groups randomly.

Exclusion criteria

Exclusion criteria: History of anesthetic allergy, puncture site infection or trauma, hard to communicate, history of mental illness or recent use of psychotropic drugs, history of analgesic drug abuse, pregnancy, unclear anatomical structure shown by ultrasound, malformed vertebrae, severe organ dysfunction.

Design outcomes

Primary

MeasureTime frame
visual analog scale, VAS;

Secondary

MeasureTime frame
intraoperative sulfentanil consumption;intraoperative remifentanil consumption;intraoperative sevoflurane consumption;postoperative sufentanil consumption for the first 48 hours;overall benefit of analgesia score, OBAS;total number of postoperative PCA attempts;postoperative remedial analgesics usage;adverse events (such as nausea, vomiting, dizziness and irritability);first anal exhaust time;length of hospitalization;hospitalization expenses;

Countries

China

Contacts

Public ContactYanwu Jin

the Second Hospital of Shandong University

xiaojin19781129@126.com+86 15806603618

Outcome results

None listed

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