Ilioinguinal/Iliohypogastric Block for Inguinal Hernia Repair

Status Not yet recruiting

Clinical Trial Summary

Inguinal hernia have traditionally been done under general anesthesia. While safe, general anesthesia is associated with potential postoperative nausea/vomiting and drowsiness. Additionally, the recent COVID19 pandemic has heightened the precaution to avoid aerosol generating procedures (AGP) if possible. General anesthesia requires airway manipulation, thus necessitate performing an AGP. Recently, we began using peripheral nerve block and sedation as primary anesthetic technique for inguinal hernia repairs. While surgeon administered local anesthetic, also known as local infiltration, has been done for inguinal hernia repair, using specific nerve blocks and sedation has not been compared with general anesthesia. We believe the advantage of this novel technique can improve postoperative recovery. This retrospective study will compare the total hospital length of stay of those receiving nerve blocks and sedation as primary anesthetic techniques versus those with general anesthesia.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05335837
Study type	Observational
Source	Lawson Health Research Institute
Contact	Cheng Lin
Phone	5196858600
Email	cheng.lin@lhsc.on.ca
Status	Not yet recruiting
Phase
Start date	May 1, 2022
Completion date	July 1, 2022

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