Overview

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

Status:
Not yet recruiting
Trial end date:
2024-01-01
Target enrollment:
0
Participant gender:
All
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
Phase:
Early Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Tanta University
Treatments:
Bupivacaine
Dexamethasone
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 repair

Exclusion Criteria:

1. Patient refusal.

2. Body mass index (BMI) >40 kg m2.

3. The presence of skin infection at the injection site.

4. Allergy to local anesthetic drugs.