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Efficacy of Esflurbiprofen transdermal patch for postoperative analgesia in multilevel posterior lumbar spinal fusion: A randomized controlled trial

Efficacy of Esflurbiprofen transdermal patch for postoperative analgesia in multilevel posterior lumbar spinal fusion: A randomized controlled trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240929002
Enrollment
56
Registered
2024-09-29
Start date
2025-04-05
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

Patients allergic or intolerant to the interventional drugs used Patients with severe liver, kidney, and cardiovascular disease Patients with open wounds or chronic skin disease such as psoriasis, chronic dermatitis etc. Esflurbiprofen transdermal patch Topical NSAID for postoperative analgesia Post-operative pain management in spinal fusion

Interventions

Esflurbiprofen transdermal patch is an anti-inflammatory preparation for topical use that contained 40 mg of Esflurbiprofen. ,Medicated plaster administration is a unique preparation that provides lo
Active Comparator Drug,Placebo Comparator Drug
Esflurbiprofen transdermal patch,Medicated plaster

Sponsors

ourself
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients > 18 years with a lumbar degenerative disease with surgical indications (including spondylolisthesis, lumbar instability, lumbar spinal stenosis, etc.) Multisegmental fusion of the lumbar spine with instrumentation (2-3 levels).

Exclusion criteria

Exclusion criteria: A history of previous lumbar surgery A history of opioids used to control pain within 30 days Patients allergic or intolerant to the interventional drugs used Patients with severe liver, kidney, and cardiovascular disease Patients with open wounds or chronic skin disease such as psoriasis, chronic dermatitis etc.

Design outcomes

Primary

MeasureTime frame
Morphine consumption the first 12 hours, between 12-24 hours, 24-48 hours Cumulative dose

Secondary

MeasureTime frame
Post-operative pain 8 hours, 16 hours, 24 hours, 36 hours, 48 hours, and 72 hours postoperatively VAS

Countries

Thailand

Contacts

Public ContactTerdpong Tanaviriyachai

Department of Orthopaedics, Maharat Nakhon Ratchasima Hospital.

bomorthokorat@gmail.com0894929655

Outcome results

None listed

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