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Inhalational Analgesic
Intervention group for Acute Pain
Phase 3
Waitlist Available
Research Sponsored by Université de Sherbrooke
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up immediately after the intervention
Awards & highlights
Study Summary
This is a randomised, double-blind, placebo controlled study to evaluate the efficacy of Methoxyflurane (Penthrox®) for the treatment of acute pain during closed nasal fracture reduction. The study aims to provide evidence under blinded controlled conditions that Penthrox is safe and effective in patients aged 18 to 65 years during closed nasal fracture reduction.
Eligible Conditions
- Acute Pain
- Broken Nose
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ immediately after the intervention
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~immediately after the intervention
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Pain level variation during nasal closed reduction: visual analog scale
Secondary outcome measures
Number of procedures limited by pain
Pain level during anesthesia: visual analog scale
Rate of participants requesting backup analgesia during the procedure
+2 moreTrial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Intervention groupExperimental Treatment1 Intervention
Inhalation of Methoxyflurane through a Penthrox inhaler
Group II: Control groupPlacebo Group1 Intervention
Inhalation of placebo (0.9% salin solution) through a Penthrox inhaler
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Who is running the clinical trial?
Université de SherbrookeLead Sponsor
292 Previous Clinical Trials
69,407 Total Patients Enrolled
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