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Does ultrasound-guided erector spinae plane block improve the quality of recovery after spinal fusion surgery?

Efficacy of ultrasound-guided erector spinae plane block on postoperative quality of recovery after spinal fusion surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027186
Enrollment
Unknown
Registered
2019-11-04
Start date
2019-11-08
Completion date
Unknown
Last updated
2022-03-07

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

Conditions

Lumbar stenosis

Interventions

experimental group:bilateral erect spinae plane block with 20 ml of 0.375% ropivacaine on each side
Control group:Sham (no ESPB)

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. Undergoing spinal fusion surgery; 3. ASA status I to III.

Exclusion criteria

Exclusion criteria: 1. Chronic pain; 2. Infection near the puncture site; 3. Having a history of NASID drug allergy and local anesthetic allergy; 4. Use of pain medications; 5. Inability to communicate, and other reasons that not appropriate for this study.

Design outcomes

Primary

MeasureTime frame
the quality of recovery;—

Secondary

MeasureTime frame
Postoperative pain intensity at rest;Postoperative pain intensity on movement;postoperative opioids consumption;postoperative nause and vomiting;the patient's satisfaction;Pruritus;Dizziness;—

Countries

China

Contacts

Public ContactYusheng Yao

Fujian Medical University

fjslyys@126.com+86 13559939629

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 18, 2026