MedPath

Ilioinguinal/Iliohypogastric Block for Inguinal Hernia Repair

Conditions
Anesthesia
Interventions
Procedure: Regional Anesthesia and Sedation
Registration Number
NCT05335837
Lead Sponsor
Lawson Health Research Institute
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
350
Inclusion Criteria
  • 18 years or older
  • American Society of Anesthesiologists (ASA) Physical Status I to III
  • Body Mass Index (BMI) less than 45
  • Single hernia repair, elective, ambulatory surgery
Exclusion Criteria
  • Opioid dependence (30 mg oral morphine equivalents daily or more)
  • History of malignant hyperthermia
  • Pregnancy

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Regional Anesthesia and SedationRegional Anesthesia and Sedationpatients received ilioinguinal/iliohypogastric nerve blocks and sedation for inguinal hernia repair
Primary Outcome Measures
NameTimeMethod
Postoperative recovery timeTime from exiting operating room to time ready for hospital discharge, up to 100 hours

Time from exiting operating room to time ready for hospital discharge

Secondary Outcome Measures
NameTimeMethod
Hospital length of stayTime from patient registration to ready for hospital discharge, up to 100 hours

Time from patient registration to ready for hospital discharge

Severe painTime from exiting operating room to time ready for hospital discharge, up to 100 hours

Any incidence when patient rated pain at least 7 out of 10 numeric rating scale

Preoperative timeTime from patient registration to entering operating room, up to 100 hours

Time from patient registration to entering operating room

Postoperative nausea vomitingTime from exiting operating room to time ready for hospital discharge, up to 100 hours

Associated symptoms of nausea vomiting, or received non-prophylactic antiemetics

DesaturationTime from exiting operating room to time ready for hospital discharge, up to 100 hours

Oxygen saturation below 90% with or without oxygen

Postoperative opioid doseTime from exiting operating room to time ready for hospital discharge, up to 100 hours

total postoperative opioid dose in oral morphine equivalents

Intraoperative timeTime from entering to exiting operating room, up to 100 hours

Time from entering to exiting operating room

Trial Locations

Locations (1)

Cheng Lin

🇨🇦

London, Ontario, Canada

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