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Neuragen® for the relief of neuropathic pain part 2: a randomised, double-blind, placebo controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN08911796
Enrollment
60
Registered
2008-06-13
Start date
2008-05-19
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 polyneuropathies

Interventions

Topical application of Neuragen® with different amounts of effective ingredients versus a placebo. The medicine was sprayed onto the subjects feet at the sole and on top of the feet. One time applicat

Sponsors

Origin BioMed, Inc. (Canada)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Male and female, over 21 years 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. 0 - 10 visual analog scale was use to document pain level at 30 minutes before and after the administration of the medication, with 8-hour follow up every hour on the hour.

Secondary

MeasureTime frame
Duration of pain reduction. 0 - 10 visual analog scale was use to document pain level at 30 minutes before and after the administration of the medication, with 8-hour follow up every hour on the hour.

Countries

United States of America

Outcome results

None listed

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