Clinical Trial

Comparing Two Nerve Block Methods for Pain Relief in Laparoscopic Hernia Surgery

Active, Not Recruiting
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Summary
After inguinal hernia repair, patients having chronic pain approximately 20 percent. If patients don't have postoperatively acute pain, they will tend to have less chronic pain. The purpose of study is to make people have less pain, even better not to have any. In this study, patients will have preemptive nerve blockage and by this way, they will have less acute and chronic pain.
Trial Details
NCT Number NCT07676123
Lead Sponsor Ankara University
Conditions MeSH C23.300.707.374.875, MeSH E01.370.388.250.520, MeSH E03.155.086.711, MeSH C23.550.767.700, MeSH C23.550.767.859
Enrollment 66 participants
Start Date 2025-06-26
Primary Completion 2026-02-26 (estimated)
Study Completion 2026-06-26 (estimated)
Updated on ClinicalTrials.gov 2026-06-30