Hernia, Inguinal Clinical Trial
Official title:
The Analgesic Efficacy of Two Bupivacaine Concentrations for Combined Ilioinguinal and Iliohypogastric Nerve Block in Postherniorrhaphy Pain.
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
Status | Not yet recruiting |
Enrollment | 90 |
Est. completion date | January 2024 |
Est. primary completion date | December 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | 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. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Tanta University |
Bugedo GJ, Carcamo CR, Mertens RA, Dagnino JA, Munoz HR. Preoperative percutaneous ilioinguinal and iliohypogastric nerve block with 0.5% bupivacaine for post-herniorrhaphy pain management in adults. Reg Anesth. 1990 May-Jun;15(3):130-3. — View Citation
Kamal K, Jain P, Bansal T, Ahlawat G. A comparative study to evaluate ultrasound-guided transversus abdominis plane block versus ilioinguinal iliohypogastric nerve block for post-operative analgesia in adult patients undergoing inguinal hernia repair. Indian J Anaesth. 2018 Apr;62(4):292-297. doi: 10.4103/ija.IJA_548_17. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The time to first request for rescue analgesia. | if score is = 3 analgesia needed | 24 hours | |
Secondary | The post-operative pain in the form of NRS. | at 0, 2, 4, 8, 12, 18 and 24 hours post-procedure. | ||
Secondary | The total 24 hour opioid consumption | 24 hours | ||
Secondary | The incidence of complication related to nerve block | urinary retention, hematoma, hypotension and arrhythmia | 48 hours | |
Secondary | Patient satisfaction | in the form of 4 point satisfaction questionnaire: where 1 would be satisfied, 2=neutral, 3=dissatisfied, and 4=extremely dissatisfied. | 48 hours |
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