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Inhaled Anesthetic
Nitrous Oxide for Obsessive-Compulsive Disorder
Phase 2
Recruiting
Led By Peter J van Roessel, MD, PhD
Research Sponsored by Stanford University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Capacity to provide informed consent
Age 18-65
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 week
Summary
This trial uses nitrous oxide gas, commonly known as laughing gas, to see if it can quickly help people with OCD. It targets individuals with OCD because they often struggle with persistent and distressing thoughts and behaviors. The gas might work by altering brain chemicals to improve mood and reduce symptoms.
Who is the study for?
This trial is for adults aged 18-65 with a primary diagnosis of OCD who have severe symptoms. Participants must be able to give informed consent and go through a treatment-free period. It's not open to those on conflicting medications, with certain psychiatric or medical conditions, or women who are pregnant or nursing.
What is being tested?
The study is testing if inhaling nitrous oxide can quickly help improve OCD symptoms compared to inhaling nitrogen (a non-active gas). The idea is that the anesthetic properties of nitrous oxide might offer rapid relief from the distress caused by OCD.
What are the potential side effects?
While generally well-tolerated, inhaled nitrous oxide may cause side effects like dizziness, nausea, headache, fatigue, and in rare cases numbness or tingling due to its anesthetic nature.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I understand and can agree to the study's procedures and risks.
Select...
I am between 18 and 65 years old.
Select...
My primary diagnosis is OCD.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 week
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 week
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Improvement in the severity of OCD symptoms as measured by the Yale-Brown Obsessive Compulsive Scale (YBOCS)
Side effects data
From 2018 Phase 4 trial • 63 Patients • NCT030855637%
hypoxia
2%
paradoxical reaction
100%
80%
60%
40%
20%
0%
Study treatment Arm
Intranasal Midazolam
Nitrous Oxide
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Experimental: Nitrous OxideExperimental Treatment1 Intervention
OCD participants in this arm will receive 50%oxygen/50% nitrous oxide admixture for 60 minutes.
Group II: Control: NitrogenPlacebo Group1 Intervention
OCD participants in this arm will receive 50%oxygen/50% nitrogen admixture for 60 minutes.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Nitrous Oxide
2016
Completed Phase 4
~8380
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Obsessive-Compulsive Disorder (OCD) include selective serotonin reuptake inhibitors (SSRIs), serotonin-norepinephrine reuptake inhibitors (SNRIs), and cognitive-behavioral therapy (CBT) with exposure and response prevention (ERP). SSRIs and SNRIs work by increasing the levels of serotonin and norepinephrine in the brain, which helps to regulate mood and reduce anxiety.
CBT, particularly ERP, helps patients confront and reduce their obsessions and compulsions through structured exposure to anxiety-provoking stimuli and prevention of the associated compulsive behaviors. Nitrous oxide, currently under investigation, may offer rapid symptom relief due to its anxiolytic and analgesic properties.
Understanding these mechanisms is crucial for patients as it helps them make informed decisions about their treatment options and manage their expectations regarding the onset and type of symptom relief.
Beyond refractory obsessions and anxiety states: toward remission.[Psychosurgery and the neurosurgical treatment of pain: a systematic review of the experience gained in these kinds of treatment].
Beyond refractory obsessions and anxiety states: toward remission.[Psychosurgery and the neurosurgical treatment of pain: a systematic review of the experience gained in these kinds of treatment].
Find a Location
Who is running the clinical trial?
Stanford UniversityLead Sponsor
2,467 Previous Clinical Trials
17,496,057 Total Patients Enrolled
16 Trials studying Obsessive-Compulsive Disorder
1,365 Patients Enrolled for Obsessive-Compulsive Disorder
Brain & Behavior Research FoundationOTHER
62 Previous Clinical Trials
2,876 Total Patients Enrolled
1 Trials studying Obsessive-Compulsive Disorder
148 Patients Enrolled for Obsessive-Compulsive Disorder
Peter J van Roessel, MD, PhD5.02 ReviewsPrincipal Investigator - Stanford Univeristy
Stanford University
1 Previous Clinical Trials
16 Total Patients Enrolled
1 Trials studying Obsessive-Compulsive Disorder
16 Patients Enrolled for Obsessive-Compulsive Disorder
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I understand and can agree to the study's procedures and risks.I am between 18 and 65 years old.I am not taking any medications that could interfere with the trial.Your medical or mental health conditions may put you at risk and it's not safe for you to participate.I can go without treatment for a while.My primary diagnosis is OCD.My OCD symptoms are severe.You are currently pregnant or nursing a baby.
Research Study Groups:
This trial has the following groups:- Group 1: Control: Nitrogen
- Group 2: Experimental: Nitrous Oxide
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Obsessive-Compulsive Disorder Patient Testimony for trial: Trial Name: NCT03826693 — Phase 2
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