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RECRUITING NA

DoD AtMS for Posttraumatic Peripheral Neuropathic Pain

NCT07301177 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this clinical trial is to learn if adaptative transcutaneous magnetic stimulation (AtMS) works to reduce pain caused by post-traumatic peripheral neuropathic pain (PTP-NP) within Veterans and/or active duty military personnel. It will also learn about the safety of AtMS. The main questions it aims to answer are: 1. What are the effects of adaptative tMS (AtMS) in alleviating patients' PTP-NP compared to fixed tMS (FtMS) and Sham-tMS? 2. What are the effects of AtMS in improving functions in patients suffering from PTP-NP compared to FtMS and Sham-tMS? 3. What are the effects of AtMS in improving mood in patients suffering from PTP NP compared FtMS and Sham-tMS? Researchers will compare AtMS, FtMS and Sham-tMS to see if AtMS is the best form of tMS in treating PTP-NP. Participants will undergo the following: 1. Receive a total of 8 AtMS, FtMS, or Sham-tMS treatments over 16 weeks. 2. Visit the clinic a total of 12 times for assessments, check ups, and treatments. 3. Keep a daily diary of their PTP-NP intensity, sleep interference, and pain medications used.

Interventions

  • DEVICE Transcutaneous magnetic stimulation (tMS)
  • DEVICE Sham transcutaneous magnetic stimulation (Sham-tMS)
  • DEVICE Patient Machine Interface (PMI)

Study Locations (1)

California

  • Veterans Medical Center - San Diego — San Diego

Trial Details

FieldValue
Enrollment Target 180 participants
Start Date 2025-04-30
Est. Completion 2029-03
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07301177

The ClinicalTrials.gov registry entry for NCT07301177 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 180 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Veterans Medical Research Foundation, which has 17 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Peripheral Neuropathy appearing as the primary indexed condition, and to 3 interventions — of which Transcutaneous magnetic stimulation (tMS) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07301177 reports 1 study location spanning 1 distinct geographic area — top geographies include California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07301177 about?

NCT07301177 is a clinical study titled "DoD AtMS for Posttraumatic Peripheral Neuropathic Pain". The goal of this clinical trial is to learn if adaptative transcutaneous magnetic stimulation (AtMS) works to reduce pain caused by post-traumatic peripheral neuropathic pain (PTP-NP) within Veterans and/or active duty military personnel. It will also learn about the safety of AtMS. The main questio...

What is the current status of trial NCT07301177?

This trial is currently recruiting. It is a NA study. The enrollment target is 180 participants. The study started on 2025-04-30. Estimated completion is 2029-03.

What conditions does trial NCT07301177 study?

This clinical trial studies the following conditions: Peripheral Neuropathy, Posttraumatic Peripheral Neuropathic Pain, Peripheral Neuropathy Due to Surgical Trauma, Peripheral Neuropathy Due to Physical Trauma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07301177?

The interventions under investigation include: Transcutaneous magnetic stimulation (tMS) (DEVICE), Sham transcutaneous magnetic stimulation (Sham-tMS) (DEVICE), Patient Machine Interface (PMI) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07301177?

This trial is sponsored by Veterans Medical Research Foundation, which has 17 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07301177 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial