Nitrous Oxide as Treatment for Fibromyalgia
Reason given: PI has left university
Key facts
- Where
- Chicago, United StatesSee the site
- Phase
- Phase 2
Where in United States
- University of ChicagoChicago, United StatesNo longer taking part
Trial details
- Who runs it
- University of Chicago
- Trial code
- NCT05357066
- Record updated
- 14 May 2026
- Original description
The purpose of this study is to explore a potential role of nitrous oxide in treating pain associated with fibromyalgia.Read full original descriptionShow less
The purpose of this study is to explore a potential role of nitrous oxide in treating pain associated with fibromyalgia.
Inclusion: 2016 American College of Rheumatology Revised criteria for fibromyalgia (2016-ACR); Subjects 18 -75 years of age; Self-reported pain of at least 4 on the Numeric Pain Rating Scale (NPRS) at screening and baseline; Subject receives and agrees to remain on their stable fibromyalgia treatment plan established at least 4 weeks prior to dosing. Stable means no change in dose or any pain medication; Ability to understand the requirements of the study, provide written informed consent, abide by the study restrictions, and agree to return for the required assessments; If currently on psychotherapy, it must have been maintained at the same frequency for 4 weeks prior to treatment.
Exclusion: Pain due to concurrent autoimmune or inflammatory disease such as rheumatoid arthritis, systemic lupus erythematosus, inflammatory bowel disease, or other chronic widespread pain condition(s) that may confound fibromyalgia pain; Current treatment with N-methyl-D-aspartate receptor (NMDAR) ligands including ketamine, amantadine, dextromethorphan, memantine, methadone, or dextropropoxyphene; Subjects who are pregnant, breast feeding, or planning to become pregnant during the course of the study and for 28 days after the final administration of investigational product; Unstable doses of allowed antidepressants or muscle relaxants or dosages for any other medical condition; Psychiatric or cognitive disorder (e.g., current schizophrenia, severe depression, suicidal ideation, dementia, etc.) that the investigator or sponsor considers significant for this study; Current or recent history of medically inappropriate or illegal use of drugs of abuse including benzodiazepines, opiates, cocaine, cannabinoids, and amphetamines; Any other serious medical condition affecting heart, lung or any other organ system; Any impairment, activity or situation that in the judgment of the investigator would prevent satisfactory completion of the study protocol; Clinically significant alcohol or other substance abuse within the last 2 years, in the opinion of the investigator.