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Evaluation of ultrasound-guided erector spinae plane block versus wound infiltration for analgesic efficacy in spinal surgery: a double-blind prospective randomized controlled study

Evaluation of ultrasound-guided erector spinae plane block versus wound infiltration for analgesic efficacy in spinal surgery: a double-blind prospective randomized controlled study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053008
Enrollment
Unknown
Registered
2021-11-08
Start date
2021-11-22
Completion date
Unknown
Last updated
2022-08-30

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

Conditions

Spine Surgery

Interventions

Bilateral ultrasound-guided erector spinae plane block group:Bilateral ultrasound-guided erector spinae plane block
Wound infiltration group:Wound infiltration

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 70 years; 2. Lumbar spinal fusion surgery is planned; 3. Agree to undergo regional nerve block or wound infiltration and postoperative intravenous controlled analgesia.

Exclusion criteria

Exclusion criteria: 1. Preoperative severe renal insufficiency (serum creatinine >442umol/L or requiring renal replacement therapy), liver insufficiency (Child-Pugh grade C), or ASA grade >= IV; 2. Chronic opioids dependence and long-term use of various types of painkillers (more than 3 months); 3. Those who cannot communicate fluently before surgery due to severe dementia, language barrier or end-stage disease; 4. Preoperative complications of central nervous system and/or peripheral nervous system diseases; 5. Allergy to local anesthetics.

Design outcomes

Primary

MeasureTime frame
Total amount of opioids used within 24 hours after surgery;

Secondary

MeasureTime frame
Postoperative NRS score at rest and active movement;Sleep quality on postoperative day;Quality of recovery 24 hours after surgery;Complications during postoperative hospitalization;Duration of postoperative hospital stay;

Countries

China

Contacts

Public ContactZhang Zhen

Peking University First Hospital

zhangzhen1st@163.com+86 13681035526

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026