Peripheral Neuropathy Trial, Recruiting NCT07301177 Sponsor: Veterans Medical Research Foundation Condition: Peripheral Neuropathy
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Peripheral Neuropathy Trial, Recruiting

NCT07301177
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Veterans (men or women) of any race or ethnicity who are 18 years of age or older
  • People who have had ongoing nerve pain in a part of the body for more than 4 months, where that pain started after an injury or surgery
  • People whose average daily pain score is greater than 3 out of 10 on a standard pain rating scale
  • People who have at least one change in sensation (such as numbness, tingling, or increased sensitivity) in the area of the body connected to the damaged nerve
  • People who have had diagnostic tests (such as scans or nerve studies) that confirm a nerve injury or condition that explains their pain

Who may not be able to join:

  • People who are pregnant
  • People whose nerve pain is caused by conditions such as diabetes, HIV, chemotherapy or antiviral treatment, carpal tunnel syndrome, or pain that originates in the brain or spinal cord rather than in a peripheral (body) nerve
  • People whose pain is caused by Complex Regional Pain Syndrome
  • People experiencing phantom limb pain following an amputation (note: stump pain and phantom sensations without pain may be allowed — confirm with trial site)
  • People who have a skin condition affecting the area of skin connected to the painful nerve
  • People who have other types of pain, such as neck or lower back nerve pain, that could make it difficult to assess results accurately
  • People who are considered to be at risk of suicide
  • People who are currently taking certain medications that are not permitted, unless an appropriate period of stopping that medication has passed beforehand
  • People who have taken part in another clinical trial within the 30 days before screening, or who are currently in another trial
  • People who have a heart pacemaker
  • People who have a currently diagnosed major psychiatric condition (note: generalised anxiety disorder and major depressive disorder may be allowed if the condition is considered clinically stable — confirm with trial site)
  • People who have an active or pending lawsuit related to the injury causing their pain
  • People who have previously received transcranial or transcutaneous magnetic stimulation therapy at any point in the past

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 19 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Albert Y Leung, M.D., Veterans Medical Research Foundation (VMRF)

Phone: 8586423146

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Veterans Medical Research Foundation
Registry
ClinicalTrials.gov
Start date
30 April 2025
Est. completion
1 November 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Neuropathic Pain Rating; Mood; Quality of Life (Sleep Interference); Functionality - Absenteeism; Functionality - Presenteeism; Functionality - Overall work Productivity Impairment; Functionality - Activity Impairment

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov