Ilioinguinal/Iliohypogastric Block for Inguinal Hernia Repair
NCT ID: NCT05335837
Last Updated: 2022-04-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
350 participants
OBSERVATIONAL
2022-05-01
2022-07-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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General Anesthesia
patients received general anesthesia for inguinal hernia repair
No interventions assigned to this group
Regional Anesthesia and Sedation
patients received ilioinguinal/iliohypogastric nerve blocks and sedation for inguinal hernia repair
Regional Anesthesia and Sedation
Preoperative ilioinguinal/iliohypogastric nerve block and moderate to deep intraoperative sedation.
Interventions
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Regional Anesthesia and Sedation
Preoperative ilioinguinal/iliohypogastric nerve block and moderate to deep intraoperative sedation.
Eligibility Criteria
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Inclusion Criteria
* 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
* History of malignant hyperthermia
* Pregnancy
18 Years
ALL
No
Sponsors
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London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
OTHER
Responsible Party
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Cheng Lin
Clinical Professor
Locations
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Cheng Lin
London, Ontario, Canada
Countries
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Central Contacts
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Facility Contacts
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Cheng Lin
Role: primary
Other Identifiers
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119564
Identifier Type: -
Identifier Source: org_study_id
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