drugset / Trial / NCT05687981

The Analgesic Efficacy of Two Bupivacaine Concentrations for Combined Ilioinguinal and Iliohypogastric Nerve Block in Postherniorrhaphy Pain

NCT05687981

Phase 0 Unknown 90 enrolled Tanta University
RandomizedParallel-groupSingle-blindTreatment

Summary

The present study will be undertaken to compare the postoperative analgesic effect of 0.25% bupivacaine and 0.5% bupivacaine for unilateral ilioinguinal and Iliohypogastric nerve block after open inguinal hernia repair. Primary outcome: The time to first request for rescue analgesia. Secondary outcome: 1. The post-operative pain in the form of NRS scores at rest \& during movement at 0, 2, 4, 8, 12, 18 and 24 hours post-procedure. 2. The total 24 hour opioid consumption. 3. The incidence of complication related to nerve block (urinary retention, hematoma, hypotension and arrhythmia). 4. Patient satisfaction

Timeline

Start
2023-01
Primary completion
2023-12
Completion
2024-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bupivacaine Other / unclassified 0.25 %
Comparator Bupivacaine Other / unclassified 0.5 %
Comparator Dexamethasone Small molecule 2 mg

Indications

No indication recorded.