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Metanx Effects on Nerve Fiber Density in Neuropathic Diabetics

Metanx Effects on Nerve Fiber Density in Neuropathic Diabetics

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01503892
Acronym
SLHN2011-18
Enrollment
100
Registered
2012-01-04
Start date
2011-12-31
Completion date
Unknown
Last updated
2012-07-17

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

Conditions

Diabetes, Peripheral Neuropathy

Keywords

Small Fiber Neuropathy, Metanx Effect on Small Fiber Neuropathy, Metanx Effect on Diabetic Peripheral Neuropathy

Brief summary

This study focuses on the use of Metanx® as the sole treatment for improving and reversing nerve damage in type 2 diabetic patients with peripheral neuropathy. There will be two equal study groups enrolled in this randomized double blinded study. The minimum sample size of enrollment is 24 (12 per group), which is required for 90% power at alpha = .05. The maximum number of participants will be set at 100 (50 per group). Patients who are pre-diabetic or patients who have been diagnosed with diabetes type II for less than five years are included in this study. The control group will receive placebo pill twice daily versus the treatment group which will receive one Metanx® tablet twice daily. Each group will have intraepidermal nerve fiber densities obtained by skin biopsies taken at the beginning of the study before any treatment has begun as well as a final intraepidermal nerve skin biopsy at the end of twelve months to re-biopsy. In addition each group will answer three sets of questionnaires relating to their peripheral neuropathy at initial, three months, twelve month visitations. If Metanx® is able to reverse nerve damage and improve symptoms then the final nerve biopsies will show an increase in intraepidermal nerve fiber density and an improvement in the subjective score versus the placebo group.

Interventions

DIETARY_SUPPLEMENTMetanx

Metanx- one tablet twice daily for twelve months

DRUGPlacebo

Placebo- one tablet twice daily for twelve months.

Sponsors

Goldfarb Foundation
CollaboratorUNKNOWN
Pamlab, L.L.C.
CollaboratorINDUSTRY
St. Luke's Hospital and Health Network, Pennsylvania
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Type 2 Diabetics * Pre-diabetics * Symptoms of peripheral neuropathy

Exclusion criteria

* Pregnancy * Under age 18 * HIV (+)

Design outcomes

Primary

MeasureTime frameDescription
Increased intraepidermal nerve fiber density1 yearIf Metanx® is able to reverse nerve damage and improve symptoms then the final nerve biopsies will show an increase in intraepidermal nerve fiber density

Secondary

MeasureTime frameDescription
Subjective improvement1 yearImprovement in the subjective score versus the placebo group.

Countries

United States

Contacts

Primary ContactEdwin S. Hart III, DPM
ehart@footmed.com610-868-4300

Outcome results

None listed

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