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Hand Held NitrousTM for Anesthesia (HHN Trial)
N/A
Waitlist Available
Led By Howard Beck, MD
Research Sponsored by Strata Medical Innovations
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
* Any patient undergoing a painful office procedure or exam
Timeline
Screening 3 weeks
Treatment Varies
Follow Up the patient is under observation for the length of the procedure or until baseline parameters are met (under 10 minutes). no followup is required.
Awards & highlights
No Placebo-Only Group
Summary
To study the safety and efficacy of Hand Held Nitrous. A device that delivers 120 seconds of up to 72% nitrous oxide and ambient air.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ the patient is under observation for the length of the procedure or until baseline parameters are met (under 10 minutes). no followup is required.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~the patient is under observation for the length of the procedure or until baseline parameters are met (under 10 minutes). no followup is required.
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
This study measures the types of complications (if any) associated with the use of small set amount of nitrous oxide.
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Hand Held NitrousTMExperimental Treatment1 Intervention
There are no other interventions to this device
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Who is running the clinical trial?
Strata Medical InnovationsLead Sponsor
Howard Beck, MDPrincipal Investigator
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