Peripheral Neuropathy Trial, Recruiting NCT06222203 Sponsor: National Cancer Institute (NCI) Condition: Peripheral Neuropathy
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Peripheral Neuropathy Trial, Recruiting

NCT06222203
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:

Main participant groups (High-Risk and Low-Risk Cohorts):

  • People aged 3 years or older.
  • People who have been diagnosed with Neurofibromatosis Type 1 (NF1), either through clinical assessment or genetic testing.
  • People with a diagnosis of mosaic or segmental NF1 (a form where only some cells or a specific area of the body is affected) are also eligible.
  • Participants are placed into a High-Risk or Low-Risk group depending on whether they have certain additional characteristics, such as specific gene variants linked to a higher risk of nerve sheath tumours, a personal or family history of certain nerve tumours, a history of radiation treatment, a large growth called a plexiform neurofibroma, or the presence of a type of lesion called a distinct nodular lesion (DNL) — (confirm with trial site for full details of which group applies).
  • The participant, or their parent, guardian, or legally authorised representative, must be willing and able to sign a consent form.

Parent/Guardian group:

  • Parents or guardians of child participants aged 8 to 17 years who are enrolled in the High-Risk or Low-Risk groups.
  • The parent, guardian, or legally authorised representative must be willing and able to sign a consent form for their own participation in this part of the study.

Who may not be able to join:

Main participant groups (High-Risk and Low-Risk Cohorts):

  • People who are unable or unwilling to have MRI scans.

Parent/Guardian group:

  • No exclusion criteria apply to this group.

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 20 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: Brigitte C Widemann, M.D., National Cancer Institute (NCI)

Phone: (240) 575-8520

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
Registry
ClinicalTrials.gov
Start date
9 October 2024
Est. completion
31 December 2034

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Assess feasibility of the study algorithm in identifying atypical neurofibromas (ANs), atypical neurofibromatous neoplasms of unknown biologic potential (ANNUBPs), CDKN2A/B mutated lesions, and/or malignant peripheral nervous sheath tumors (MPNS...

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: 20 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