Life Cycle Assessment of Different Types of Anesthetic

Sponsor
University of Alberta (Other)
Overall Status
Recruiting
CT.gov ID
NCT05385367
Collaborator
(none)
90
2
3
29
45
1.6

Study Details

Study Description

Brief Summary

Following Ethics approval, all adult patients undergoing surgery to fix the wrist fracture will be approached and consent to undergo this study. The amount of waste generated from general anesthetic, regional anesthetic and regional+general anesthetic will be collected and weighed.

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Regional anesthetic
  • Other: General anesthetic
  • Other: Combined general anesthetic and regional anesthetic
N/A

Detailed Description

Following Ethics approval, all adult patients undergoing surgery to fix the wrist fracture will be approached and consent to undergo this study. The amount of waste generated from general anesthetic, regional anesthetic and regional+general anesthetic will be collected and weighed. Waste will include disposable and reusable wastes. Examples of disposable waste are all plastic packaging, syringes, needles, breathing tube, breathing circuits, gloves as well as drugs. Examples of reusable waste will be anesthetic face mask, laryngeal mask (which is a form of airway device that can be reprocessed), sterile gowns. The amount of anesthetic gas used will be obtained from the anesthetic machine.

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
90 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Mulicentre trialMulicentre trial
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Life Cycle Assessment of General Anesthetic, Regional Anesthetic and the Combination of General Anesthetic and Regional Anesthetic: a Randomized Controlled Trial
Actual Study Start Date :
Aug 2, 2022
Anticipated Primary Completion Date :
Dec 31, 2024
Anticipated Study Completion Date :
Dec 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Other: Regional anesthetic

Patients only have nerve block with or without sedation

Other: Regional anesthetic
Patient having just the nerve block for surgery

Other: General anesthetic

Patients only have general anesthetic

Other: General anesthetic
Patient having just general anesthetic ie. 'go completely under' for surgery

Other: Combined general anesthetic and regional anesthetic

Patients have both general anesthetic and regional anesthetic together

Other: Combined general anesthetic and regional anesthetic
Patient having a combination of a nerve block and general anesthetic for surgery

Outcome Measures

Primary Outcome Measures

  1. Carbon dioxide emission [During surgical intervention]

    Amount of carbon dioxide emission

Secondary Outcome Measures

  1. Generation of solid waste [During surgical intervention]

    Solid waste generated within the type of anesthetic

  2. Duration of surgery [During surgical intervention]

    Duration of surgery

Eligibility Criteria

Criteria

Ages Eligible for Study:
19 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • All adult patients undergoing open reduction and internal fixation of wrist

  • ASA 1-3

Exclusion Criteria:
  • no contraindications for general anesthetic in the group for general anesthetic and vice versa

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Alberta Hospital Edmonton Alberta Canada T6G 2B7
2 Sturgeon Community Hospital St. Albert Alberta Canada T8N 6C4

Sponsors and Collaborators

  • University of Alberta

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Alberta
ClinicalTrials.gov Identifier:
NCT05385367
Other Study ID Numbers:
  • Pro00118522
First Posted:
May 23, 2022
Last Update Posted:
Aug 19, 2022
Last Verified:
Aug 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Alberta
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 19, 2022