Actively Recruiting

Age: 14Years - 65Years
All Genders
ID05540561

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

Age: 14Years - 65Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

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

Actively Recruiting

3

CALAIS

Calais, France

Actively Recruiting

4

Lens

Lens, France

Actively Recruiting

5

Chu Lille

Lille, France

Actively Recruiting

6

Nantes

Nantes, France

Actively Recruiting

7

Roubaix

Roubaix, France

Actively Recruiting

8

Rouen

Rouen, France

Actively Recruiting

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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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