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Disinfectant

Alcohol for Skin Infections

Phase 3
Waitlist Available
Led By Anna Taddio, PhD
Research Sponsored by University of Toronto
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
healthy pediatric patients undergoing routine vaccinations
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from date of first enrollment until the date of final enrollment, up to 1 year
Awards & highlights

Study Summary

Alcohol is used to disinfect the skin prior to injections in order to prevent infections caused by bacteria on the skin being injected within tissue. At present, however, clinical trials do not demonstrate a clinical impact of using or not using alcohol swabs on infections and infection symptoms calling into question the practice of using it prior to all injections. These studies are methodologically flawed, and do not specifically examine vaccine injections. The present study is being undertaken to provide some preliminary data for the risk of infection and infection symptoms when alcohol swabs are not used to perform vaccine injections.

Eligible Conditions
  • Skin Infections

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from date of first enrollment until the date of final enrollment, up to 1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and from date of first enrollment until the date of final enrollment, up to 1 year for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Skin infection
Secondary outcome measures
Compliance with protocol
Feasibility of protocol
Feasibility of recruitment
+1 more

Side effects data

From 2017 Phase 2 trial • 17 Patients • NCT01779024
59%
Increased Appetite
41%
Somnolence
35%
Euphoric mood
29%
Fatigue
12%
Memory impairment
12%
Hyperhidrosis
12%
Dizziness
12%
Nausea
6%
Feeling hot
6%
Flushing
6%
Headache
6%
Decreased appetite
100%
80%
60%
40%
20%
0%
Study treatment Arm
Ghrelin
Placebo

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: AlcoholExperimental Treatment1 Intervention
Alcohol will be wiped on the vaccine injection site immediately before vaccine injection.
Group II: No alcoholPlacebo Group1 Intervention
Alcohol will be wiped adjacent to the vaccine injection site immediately before vaccine injection.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Ethanol
FDA approved

Find a Location

Who is running the clinical trial?

University of TorontoLead Sponsor
690 Previous Clinical Trials
1,019,473 Total Patients Enrolled
Anna Taddio, PhDPrincipal InvestigatorUniversity of Toronto
16 Previous Clinical Trials
18,510 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~21 spots leftby Apr 2025