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A randomised trial for erector spinae plane block for analgesia after video-assisted thoracoscopic surgery

A randomised trial for erector spinae plane block for analgesia after video-assisted thoracoscopic surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018839
Enrollment
Unknown
Registered
2018-10-13
Start date
2018-10-15
Completion date
Unknown
Last updated
2019-01-28

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

Conditions

Postoperative analgesia

Interventions

EPB group:erector spinae plane block
control:No regional nerve block operation

Sponsors

Shanghai Pulmonary Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 80 years old; 2. BMI<30kg/m2; 3. Weight=40kg; 4. ASA I, II; 5. scheduled for elective thoracoscopic surgery.

Exclusion criteria

Exclusion criteria: 1. infection at local block site; 2. allergy to local anesthetics; 3. preexisting neurological deficit or psychiatric illness; 4. liver failure; 5. serum creatinine > 1.5 mg/dl; 6. chronic pain or chronic opioid use; 7. history of alcoholism or drug abuse; 8. pregnancy and inability to accomplish the pain assessment.

Design outcomes

Primary

MeasureTime frame
the worst NRS pain scores;—

Secondary

MeasureTime frame
total intra-operative sufentanil consumption;per hour, per kilogram intra-operative sufentanil consumption;—

Countries

China

Contacts

Public ContactWen Zongmei

Shanghai Pulmonary Hospital

wzm1103@126.com+86 13761635280

Outcome results

None listed

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