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OpenTrials
Completed

NCT Number: NCT05385367

Life Cycle Assessment of Different Types of Anesthetic

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.

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Key information

Age range

19 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Alberta Hospital, Edmonton, Alberta, Canada

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Regional anesthetic

Other

Patient having just the nerve block for surgery

General anesthetic

Other

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

Combined general anesthetic and regional anesthetic

Other

Patient having a combination of a nerve block and general anesthetic for surgery

Primary outcomes

  1. Carbon dioxide emission

    Time frame: During surgical intervention

    Amount of carbon dioxide emission

Secondary outcomes

  1. Generation of solid waste

    Time frame: During surgical intervention

    Solid waste generated within the type of anesthetic

  2. Duration of surgery

    Time frame: During surgical intervention

    Duration of surgery

Sponsors and collaborators

Lead sponsor

University of Alberta

Other

Registry information

Official study title

Life Cycle Assessment of General Anesthetic, Regional Anesthetic and the Combination of General Anesthetic and Regional Anesthetic: a Randomized Controlled Trial

Important dates

Study start
2022
Primary completion
2026
Study completion
2026
First posted
May 23, 2022
Registry last updated
May 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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