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Postoperative analgesic efficacy of erector spinae plane block for lumbar spinal surgery

Postoperative analgesic efficacy of erector spinae plane block for lumbar spinal surgery

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20190311002
Enrollment
62
Registered
2019-03-11
Start date
2019-03-19
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

lumbar spine surgery erector spinae plane block lumbar spine surgery postoperative morphine consumption postoperative pain

Interventions

no treatment (block),Bilateral ESPB under ultrasound guidance at 3rd lumbar spine level with 0.375%bupivacaine 20 mL
No Intervention No treatment,Active Comparator Procedure/Surgery
no ESPB block,ESPB

Sponsors

Faculty of medicine, Khon Kaen University, Thailand
Lead Sponsor
Khon Kaen university
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: age 18-75 years ASA physical status 1-3 understand and can operate the IV PCA device

Exclusion criteria

Exclusion criteria: previous lumbar spine surgery allergy to study drugs chronic used of opioids coagulopathy

Design outcomes

Primary

MeasureTime frame
Morphine consumption 0,6,12, 24,48 hour, postoperatively data from IV PCA device—

Secondary

MeasureTime frame
postoperative pain score 0,6,12, 24,48 hour, postoperatively self reported numeric rating pain score—

Contacts

Public ContactAumjit Wittayapairoj

Khon Kaen University

aumjit69@yahoo.com0815444670

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026