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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RECRUITING
NA
90 participants
INTERVENTIONAL
2022-08-02
2026-12-31
Brief Summary
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Patients undergoing this type of wrist surgery have only regional anesthetic, or general anesthetic, or both ie. regional anesthetic and general anesthetic.
The aim of the study is to compare the amount of waste generated from each type of anesthetic and this will give us a better idea of which anesthetic is more environmentally sustainable.
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Detailed Description
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Patients undergoing this type of wrist surgery have only regional anesthetic (freezing performed higher up in the arm to numb the whole arm for several hours), or general anesthetic (patient completely goes to deep anesthetic sleep), or both ie. regional anesthetic (freezing just for pain control afterwards) and general anesthetic (patient goes to deep anesthetic sleep after the freezing is done and they may need less pain killer during the surgery as well as afterwards).
The amount of waste generated will be compared amongst these 3 groups by life cycle analysis.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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Regional anesthetic
Patients only have nerve block with or without sedation
Regional anesthetic
Patient having just the nerve block for surgery
General anesthetic
Patients only have general anesthetic
General anesthetic
Patient having just general anesthetic ie. 'go completely under' for surgery
Combined general anesthetic and regional anesthetic
Patients have both general anesthetic and regional anesthetic together
Combined general anesthetic and regional anesthetic
Patient having a combination of a nerve block and general anesthetic for surgery
Interventions
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Regional anesthetic
Patient having just the nerve block for surgery
General anesthetic
Patient having just general anesthetic ie. 'go completely under' for surgery
Combined general anesthetic and regional anesthetic
Patient having a combination of a nerve block and general anesthetic for surgery
Eligibility Criteria
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Inclusion Criteria
* ASA 1-3
Exclusion Criteria
19 Years
ALL
No
Sponsors
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University of Alberta
OTHER
Responsible Party
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Locations
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University of Alberta Hospital
Edmonton, Alberta, Canada
Sturgeon Community Hospital
St. Albert, Alberta, Canada
Countries
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Facility Contacts
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Other Identifiers
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Pro00118522
Identifier Type: -
Identifier Source: org_study_id
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