Actively Recruiting
Biological Alterations of Laughing Gas Outcomes in Neurology: Monitoring Chronic Nitrous Oxide Abuse
Led by University Hospital, Lille · Updated on 2026-05-19
356
Participants Needed
8
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying the biological effects and monitoring methods of chronic nitrous oxide abuse, which can cause neurological problems such as combined sclerosis of the spinal cord. Patients may experience walking difficulties, abnormal sensations, and in severe cases may require a wheelchair. There have also been reports of thrombosis linked to nitrous oxide use. Traditional tests measuring nitrous oxide levels in blood or urine are not reliable due to the gas's short half-life, so other markers like vitamin B12 and homocysteine are being evaluated. The underlying causes of these clinical effects are not yet fully understood. The study observes two groups of nitrous oxide users: those hospitalized with clinical symptoms assessed by neurological evaluation (using the Peripheral Neuropathy Disability score) or thrombotic events, and those without clinical symptoms seen during routine medical consultations. Participants undergo blood collections for biological analysis, with samples preserved for further study. This is an observational study without experimental treatment. Participants will have blood tests at the start and at intervals up to six months to measure markers related to nitrous oxide use and clinical outcomes. Researchers will also assess nitrous oxide consumption through self-reporting and estimation, alongside the severity of related clinical signs. The main outcome is the change in blood markers over about one year. The study includes people aged 14 to 65 who currently or formerly use nitrous oxide and have social insurance coverage.
CONDITIONS
Brief Title
Biological Diagnosis and Monitoring of Chronic Nitrous Oxide Abuse
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Current or former recreational nitrous oxide user
- With or without clinical signs related to nitrous oxide use
- With or without clinico-biological aftereffects from use
- Consent to participate in the study
- Have social insurance coverage
You will not qualify if you...
- Pregnant or breastfeeding women
- Never used nitrous oxide or stopped using it more than 6 months ago
- Lack of social security coverage
- Unwilling to participate in the entire study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 year
Participants undergo blood collection and assessments of nitrous oxide consumption and clinical signs over time.
Visits at baseline, 4 weeks, 3 months, and 6 months
Trial Site Locations
Total: 8 locations
1
BETHUNE
Béthune, France
Actively Recruiting
2
Boulogne Sur Mer
Boulogne-sur-Mer, France
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3
CALAIS
Calais, France
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4
Lens
Lens, France
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5
Chu Lille
Lille, France
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6
Nantes
Nantes, France
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7
Roubaix
Roubaix, France
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8
Rouen
Rouen, France
Actively Recruiting
Research Team
G
Guillaume Grzych, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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