Treatment of Suicidal Ideation in the Emergency Department Using Nitrous Oxide
NCT ID: NCT06430489
Last Updated: 2024-06-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
PHASE2
30 participants
INTERVENTIONAL
2024-06-30
2026-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Medical air administration
Medical air
inhaled medical air (1 hour)
Nitrous oxide administration
Nitrous oxide
inhaled nitrous oxide (1 hour at 50% concentration)
Interventions
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Nitrous oxide
inhaled nitrous oxide (1 hour at 50% concentration)
Medical air
inhaled medical air (1 hour)
Eligibility Criteria
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Inclusion Criteria
* Beck Scale for Suicidal Ideation score greater than or equal to 8
* French speaking
* Patient admitted to psychiatric emergency department
* Capable of wearing a facial mask
* Having signed an informed consent
* Affiliated with social security
Exclusion Criteria
* Pregnancy or breastfeeding
* Contraindication to the use of nitrous oxide
* Legal incapacity
* Participation in another drug clinical trial
* Patient subject to compulsory care measures
18 Years
50 Years
ALL
No
Sponsors
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University Hospital, Tours
OTHER
Responsible Party
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Principal Investigators
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ANAIS VANDEVELDE, MD, PHD
Role: PRINCIPAL_INVESTIGATOR
CHRU de Tours
Locations
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Psychiatric Emergencies
Tours, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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DR230123
Identifier Type: -
Identifier Source: org_study_id
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