Clinical observation of the application of erector spinalis plane block in postoperative multimodal analgesia in patients undergoing posterior lumbar surgery

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000041433

Enrollment

Unknown

Registered

2020-12-26

Start date

2020-12-11

Completion date

Unknown

Last updated

2021-03-15

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

Conditions

Lumbar spondylolisthesis, lumbar disc herniation

Interventions

ESPB group:Plane block of erector spinalis muscle

control group:General anesthesia

Eligibility

Sex/Gender

All

Age

55 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. 60 patients underwent posterior lumbar fusion; 2. ASA grade of anesthesia was II-III; 3. Patients aged from 18 to 65 years; 4. Voluntary patients, and signed informed consent. 5. Patients receiving EspB have good compliance.

Exclusion criteria

Exclusion criteria: 1. Patients taking NSAIDs, opioids, antidepressants and anticonvulsants for a long time. 2. Patients with other mental disorders. 3. Patients who are disgusted with EspB and have poor compliance. 4. Patients with severe cardiopulmonary or hepatorenal dysfunction. 5. Patients with language or hearing impairment.

Design outcomes

Primary

Measure	Time frame
Intraoperative sufentanil dosage;Intraoperative remifentanil dosage;Visual analogue pain score at immediate, 12, 24, and 48 h after operation;Additional times of PCEA;Other remedial analgesia;	—

Secondary

Measure	Time frame
Related adverse reactions (nausea, vomiting, respiratory depression);Complications related to block (puncture site infection, hematoma, local anesthetic poisoning;	—

Countries

China

Contacts

Public ContactGao Chengjie

The 960th Hospital of PLA

Chengjiegao@hotmail.com+86 133589108967

Outcome results

None listed

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