Clinical Trial

Palmitoylethanolamide vs Ibuprofen for Pain After ESWL

Not Yet Recruiting
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Record status
This record was last updated January 5, 2026 (before its estimated June 1, 2026 completion). Its status may not reflect the trial's current state.
Summary
Pain after extracorporeal shock wave lithotripsy (ESWL), a non-surgical procedure used to treat kidney stones, is common and is usually treated with non-steroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen. However, NSAIDs may cause side effects in some patients, including stomach irritation and kidney problems. Palmitoylethanolamide (PEA) is a naturally occurring substance in the body with anti-inflammatory and pain-relieving properties and has been shown to be safe in previous studies. This study aims to compare the effectiveness of PEA with ibuprofen for controlling acute postoperative pain after ESWL. Participants undergoing ESWL will be randomly assigned to receive either oral PEA or oral ibuprofen. Pain intensity will be measured using a visual analogue scale during the first 24 hours after the procedure. The use of rescue pain medication and any side effects will also be recorded. The results of this study may help determine whether PEA can be an effective alternative to ibuprofen for the management of acute pain after ESWL.
Trial Details
NCT Number NCT07316660
Lead Sponsor Benha University
Conditions Pain After Extracorporeal Shock Wave Lithotripsy, Palmitoylethanolamide
Enrollment 120 participants
Start Date 2026-01-01
Primary Completion 2026-06-01 (estimated)
Study Completion 2026-07-01 (estimated)
Updated on ClinicalTrials.gov 2026-01-05