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The effect of Neuragen® on neuropathic pain: Double-blind, placebo-controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN20181108
Enrollment
60
Registered
2008-06-09
Start date
2007-10-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Peripheral neuropathy Nervous System Diseases Other disorders of nervous system in diseases classified elsewhere

Interventions

Topical application of Neuragen® vs placebo. Neuragen®/placebo is applied once each in random order and in a double-blind fashion. The applications are at least one week apart form each other. Pain is

Sponsors

Origin BioMed, Inc. (Canada)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Both males and females, over 21 2. Diagnosed neuropathic pain for more three months 3. Pain level between 3-8 on a 0-10 visual pain scale 4. Does not have mental and communication impairments

Exclusion criteria

Exclusion criteria: 1. Pregnant 2. Have other types of pain 3. Skin condition 4. Central nerve impairment

Design outcomes

Primary

MeasureTime frame
Foot sole pain on 11-point numerical pain scale, measured 30 minutes before and after the Neuragen®/placebo application, and tracked every hour for 8 hours.

Secondary

MeasureTime frame
Duration of pain reduction. Pain is measured 30 minutes before and after the application, and tracked every hour for 8 hours.

Countries

United States of America

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026