Ultrasound and blood markers may unlock personalized treatment for rare nerve disease

NCT ID NCT07719153

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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Status unknown
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First seen Jul 22, 2026 · Last updated Jul 23, 2026 · Updated 1 time

Summary

This study investigates whether nerve ultrasound patterns and biomarkers in blood and spinal fluid can predict how people with chronic inflammatory demyelinating polyneuropathy (CIDP) respond to treatment. Researchers will follow 30 adults with CIDP, including newly diagnosed and treatment-resistant cases, to see if imaging and lab results match clinical outcomes. The goal is to develop a strategy for more personalized care.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could lead to a way to predict which CIDP patients will respond to standard treatments, enabling more personalized and effective care.
What could go wrong
This is a small, early observational study, so findings may not apply to all CIDP patients. It is not testing a new treatment, only exploring potential markers.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 30 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Sep 2029

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population will consist of 30 consecutive adult patients with CIDP followed at the Peripheral Nervous System and Muscle Department of CHU Nice. The cohort will include 20 treatment-naïve patients with newly diagnosed CIDP enrolled before initiation of immunomodulatory therapy and 10 patients with established refractory CIDP and persistent clinically relevant disability despite adequate prior treatment. All participants will be assessed within the standard diagnostic and therapeutic care pathway for CIDP.

Ages

18 to 90 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Male or female aged 18 years or older. * Diagnosis of CIDP according to the 2021 EAN/PNS criteria; eligible phenotypes include typical CIDP, asymmetric CIDP (MADSAM/Lewis-Sumner syndrome), and pure motor CIDP. Pure sensory CIDP is excluded. * Ability to undergo protocol assessments, including clinical evaluation, electrophysiological studies, nerve ultrasound, and blood sampling. * Ability to provide written informed consent. * Affiliation with a health insurance system or equivalent. Group 1-specific criteria: * Newly diagnosed CIDP. * No previous immunomodulatory treatment for CIDP before baseline study assessment. * Planned initiation of IVIg according to standard clinical practice. Group 2-specific criteria: * Established CIDP with persistent clinically relevant disability. * Documented inadequate, partial, transient, or absent response despite adequate prior therapy, according to the final refractory disease definition. * Stable treatment exposure before inclusion according to the final protocol. Exclusion Criteria: * Pure sensory CIDP. * Alternative cause of neuropathy, including hereditary, metabolic, toxic, or other acquired neuropathies judged to better explain the clinical picture. * Motor neuron disease, myopathy, neuromuscular junction disorder, or another neurological or neuromuscular condition interfering with clinical, electrophysiological, or ultrasound interpretation. * CIDP mimic or alternative diagnosis. * Active infection likely to influence study assessments. * Active malignancy or other major systemic condition likely to confound biomarker interpretation. * Concomitant autoimmune or inflammatory disease likely to materially influence cytokine or complement measurements. * Severe psychiatric or cognitive disorder interfering with participation. * Participation in another interventional trial when incompatible with the present protocol. * Inability or unwillingness to comply with study procedures.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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