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The Effect of N2O on Chronic Neuropathic Pain Patients

The Effect of N2O on Chronic Neuropathic Pain

Status
UNKNOWN
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02246517
Acronym
N2O
Enrollment
20
Registered
2014-09-22
Start date
2014-09-30
Completion date
Unknown
Last updated
2014-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neuropathic Pain

Brief summary

Important pharmacological agents for treatment of chronic neuropathic pain such as ketamine block NMDA receptors. Nitrous oxide, an inhalant agent used extensively In anesthesia, also have antagonist property of NMDA receptors. The investigators hypothesize that prolonged treatment with N2O can alleviate chronic neuropathic pain of different causes (e.g. diabetic neuropathy, post herpetic neuralgia etc.).

Detailed description

Important pharmacological agents for treatment of chronic neuropathic pain such as ketamine block NMDA receptors. Nitrous oxide, an inhalant agent used extensively In anesthesia, also have antagonist property of NMDA receptors. The investigators hypothesize that prolonged treatment with N2O can alleviate chronic neuropathic pain of different causes (e.g. diabetic neuropathy, post herpetic neuralgia etc.). In order to examine our theory we Will recruit 40 patients aged 18-65 that suffer from chronic neuropathic pain. The patients will be divided to two groups of which half will receive treatment with N2O and half with placebo (pure O2) as a repeated weekly treatment for 4 weeks. At the beginning of the each session the patient will be asked to fill questionnaires regarding their pain quality and severity

Interventions

DRUGN2O
DRUGOxygen

Sponsors

Tel-Aviv Sourasky Medical Center
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* men and women at the age 18-65 * patient that suffer from chronic neuropathic pain * VAS\>40 * DN4 score \>4 * takes pain medication on a regular basis * Didn't get epidural injection for the pas month * signed an informed consent form

Exclusion criteria

* patients that suffer from chronic lung disease. * patients with cancer * patients with heart disease * pregnant and lactate woman * patients that suffer from depression

Design outcomes

Primary

MeasureTime frameDescription
change in adult pain as measured by visual Analog Scale for Pain (VAS Pain)baseline and average of week for 4 weeksAssessment of pain in the last 24 hours before the visit by VAS

Secondary

MeasureTime frameDescription
change in adult pain as measured by Short-Form McGill Pain Questionnaire (SF-MPQ)baseline and average of week for 4 weeksAssessment of pain in the last 24 hours before the visit by SF-MPQ

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026