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Ilioinguinal/Iliohypogastric Block for Inguinal Hernia Repair

Postoperative Recovery Time in Inguinal Hernia Repair Under Ilioinguinal, Iliohypogastric Nerve Block and Sedation Versus General Anesthesia: a Propensity Score Matched-cohort Retrospective Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05335837
Enrollment
350
Registered
2022-04-19
Start date
2022-05-01
Completion date
2022-07-01
Last updated
2022-04-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia

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.

Interventions

PROCEDURERegional Anesthesia and Sedation

Preoperative ilioinguinal/iliohypogastric nerve block and moderate to deep intraoperative sedation.

Sponsors

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

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

Design outcomes

Primary

MeasureTime frameDescription
Postoperative recovery timeTime from exiting operating room to time ready for hospital discharge, up to 100 hoursTime from exiting operating room to time ready for hospital discharge

Secondary

MeasureTime frameDescription
Preoperative timeTime from patient registration to entering operating room, up to 100 hoursTime from patient registration to entering operating room
Intraoperative timeTime from entering to exiting operating room, up to 100 hoursTime from entering to exiting operating room
Hospital length of stayTime from patient registration to ready for hospital discharge, up to 100 hoursTime from patient registration to ready for hospital discharge
Postoperative nausea vomitingTime from exiting operating room to time ready for hospital discharge, up to 100 hoursAssociated symptoms of nausea vomiting, or received non-prophylactic antiemetics
Severe painTime from exiting operating room to time ready for hospital discharge, up to 100 hoursAny incidence when patient rated pain at least 7 out of 10 numeric rating scale
DesaturationTime from exiting operating room to time ready for hospital discharge, up to 100 hoursOxygen saturation below 90% with or without oxygen
Postoperative opioid doseTime from exiting operating room to time ready for hospital discharge, up to 100 hourstotal postoperative opioid dose in oral morphine equivalents

Countries

Canada

Contacts

Primary ContactCheng Lin
cheng.lin@lhsc.on.ca5196858600

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026