Peripheral Neuropathy Trial, Recruiting NCT07319156 Sponsor: Marmara University Condition: Peripheral Neuropathy
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Peripheral Neuropathy Trial, Recruiting

NCT07319156
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:

  • People who are between 18 and 65 years old
  • People who have been diagnosed with radiating pain (pain that travels down the arm or shoulder from the neck) based on a physical examination and an MRI scan of the neck
  • People whose neck MRI shows a herniated disc (a disc in the spine that has shifted out of place) at one or more levels that matches their symptoms
  • People who are willing to take part in the study

Who may not be able to join:

  • People who have had physical therapy for their neck in the past year
  • People who have symptoms or a diagnosis of a trapped or compressed nerve in the arm or hand
  • People whose medical records show a confirmed vitamin B12 or vitamin D deficiency within the last 2 years
  • People who have previously had surgery on their neck or experienced a neck injury
  • People who have previously had surgery on their arm or hand, or experienced an arm or hand injury
  • People who have an intellectual disability
  • People who have a serious psychiatric condition
  • People who have been diagnosed with polyneuropathy (a condition affecting multiple nerves throughout the body)
  • People who have been diagnosed with diabetes
  • People who have been diagnosed with fibromyalgia (a condition causing widespread pain and fatigue)
  • People who are taking medications that may affect their sense of balance or body position (confirm with trial site)
  • People who are pregnant
  • People who do not wish to give formal consent to participate

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 28 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: Fatma B Akdağ, Research Assistant, Marmara University Faculty of Medicine ,Marmara University, Department of Physical Medicine and Rehabilitation

Phone: +90 537 452 96 60

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
Marmara University
Registry
ClinicalTrials.gov
Start date
20 December 2025
Est. completion
10 December 2026

Where this trial is recruiting

Turkey (Türkiye)

Primary endpoints

The Upper Limb Proprioception Reaching Test (PRO-Reach)

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: 28 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