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Not Yet Recruiting NCT05687981

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

Conditions: Hernia, Inguinal

Sex: All
Ages: 18 Years – 60 Years
Healthy volunteers: 1
Phase: EARLY_PHASE1
Enrollment: 90
Sponsor: Tanta University

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: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.The total 24 hour opioid consumption.The incidence of complication related to nerve block (urinary retention, hematoma, hypotension and arrhythmia).Patient satisfaction

Eligibility Criteria

Inclusion Criteria:Patients between 21 and 60 years age with the American Society of Anesthesiologists' status I or II scheduled for elective primary open inguinal hernia repairExclusion Criteria:Patient refusal.Body mass index (BMI) >40 kg m2.The presence of skin infection at the injection site.Allergy to local anesthetic drugs.

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05687981). StuddyBuddy aggregates publicly available trial information.