Ultrasound and blood markers may unlock personalized treatment for rare nerve disease
NCT ID NCT07719153
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
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2029
An estimate. End dates often move.
- Lead sponsor
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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
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18 to 90 years
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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