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Anesthetic Types for Carbon Footprint Reduction

N/A
Recruiting
Research Sponsored by University of Alberta
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
All adult patients undergoing open reduction and internal fixation of wrist
ASA 1-3
Timeline
Screening 3 weeks
Treatment Varies
Follow Up during surgical intervention
Awards & highlights

Study Summary

This trial will help determine which type of anesthesia is more environmentally sustainable.

Who is the study for?
This trial is for adult patients with a wrist fracture who are undergoing surgery and fall within the ASA physical status classification of 1-3, indicating they're fit for anesthesia. Patients must not have any contraindications to the type of anesthetic they would receive.Check my eligibility
What is being tested?
The study compares environmental impacts by measuring waste from three types of anesthesia: regional, general, and a combination of both. It aims to determine which method produces less waste and is more sustainable for surgeries like wrist fracture repairs.See study design
What are the potential side effects?
While this study focuses on environmental impact rather than medical side effects, typical risks associated with anesthetics include allergic reactions, nausea, sore throat (from intubation in general anesthesia), or nerve damage (rarely with regional).

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am an adult having surgery to fix a broken wrist with plates and screws.
Select...
My health is good to moderately impaired.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~during surgical intervention
This trial's timeline: 3 weeks for screening, Varies for treatment, and during surgical intervention for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Carbon dioxide emission
Secondary outcome measures
Duration of surgery
Generation of solid waste

Trial Design

3Treatment groups
Experimental Treatment
Group I: Regional anestheticExperimental Treatment1 Intervention
Patients only have nerve block with or without sedation
Group II: General anestheticExperimental Treatment1 Intervention
Patients only have general anesthetic
Group III: Combined general anesthetic and regional anestheticExperimental Treatment1 Intervention
Patients have both general anesthetic and regional anesthetic together

Find a Location

Who is running the clinical trial?

University of AlbertaLead Sponsor
889 Previous Clinical Trials
385,044 Total Patients Enrolled

Media Library

Combined general anesthetic and regional anesthetic Clinical Trial Eligibility Overview. Trial Name: NCT05385367 — N/A
Carbon Footprint Research Study Groups: Regional anesthetic, General anesthetic, Combined general anesthetic and regional anesthetic
Carbon Footprint Clinical Trial 2023: Combined general anesthetic and regional anesthetic Highlights & Side Effects. Trial Name: NCT05385367 — N/A
Combined general anesthetic and regional anesthetic 2023 Treatment Timeline for Medical Study. Trial Name: NCT05385367 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is the recruitment size of this trial?

"Affirmative. Information available on clinicaltrials.gov indicates that recruitment for this trial is ongoing since it was initially posted August 2nd, 2022 and last updated on the 17th of August. 90 individuals must be recruited from two separate centres to complete the study."

Answered by AI

Are there vacancies available for this trial's participants?

"According to the clinicaltrials.gov database, this trial is actively recruiting participants and was originally posted on August 2nd 2022 with a recent update made on August 17th 2022."

Answered by AI
~26 spots leftby Dec 2024