Clinical Trial

Comparison of The Continous Suprainguinal Fascia Iliaca Compartment Block and Continous Epidural

Enrolling by Invitation
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Record status
This record was last updated October 15, 2024 (before its estimated October 30, 2024 completion). Its status may not reflect the trial's current state.
Summary
This study evaluates the effectiveness of postoperative analgesia quality, Interleukin-6, Hemodynamic stability and QoR-40 of continuous Suprainguinal Fascia Iliaca Compartment Block (S-FICB) compared with continuous epidural in patients undergoing cephalomedullary nailing surgery. Half of participants will receive continuous S-FICB with patient control regional analgesia using ropivacaine 0.2% continue 2ml/hr and demand dose 5ml as needed, while the other half will receive continuous epidural with patient control epidural analgesia using same regimen.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-10-09.
Trial Details
NCT Number NCT06636331
Lead Sponsor Udayana University
Conditions Pain, Postoperative
Enrollment 46 participants
Start Date 2024-09-20
Primary Completion 2024-10-30 (estimated)
Study Completion 2024-10-30 (estimated)
Updated on ClinicalTrials.gov 2024-10-15