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Ultrasound-driven Stratification in CIDP (TAILOR-CIDP)

17. Juli 2026 aktualisiert von: Centre Hospitalier Universitaire de Nice

Ultrasound-driven Stratification in CIDP: A Prospective Observational Study Integrating Imaging and Circulating Biomarkers

Chronic inflammatory demyelinating polyradiculoneuritis (CIDP) is a rare autoimmune neuropathy characterized by significant clinical and therapeutic heterogeneity. Despite the availability of effective treatments, the response to intravenous immunoglobulins remains highly variable, and there are currently no validated biomarkers that can predict this response.

At the same time, high-resolution nerve ultrasound now makes it possible to identify different morphological profiles that may reflect distinct pathophysiological mechanisms.

This prospective, observational, single-center study, conducted at the Nice University Hospital, aims to determine whether nerve ultrasound profiles are associated with therapeutic response, clinical severity, and various biomarkers in the blood and cerebrospinal fluid. It includes two predefined cohorts: 20 patients with newly diagnosed PIDC, enrolled before the initiation of immunomodulatory treatment (Group 1), and 10 patients with refractory PIDC and clinically significant disability despite adequate prior treatment (Group 2). The ultimate goal is to develop a stratification strategy that will enable more personalized care for patients with PIDC.

Studienübersicht

Studientyp

Beobachtungs

Einschreibung (Geschätzt)

30

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studieren Sie die Kontaktsicherung

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Probenahmeverfahren

Nicht-Wahrscheinlichkeitsprobe

Studienpopulation

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.

Beschreibung

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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

Kohorten und Interventionen

Gruppe / Kohorte
Intervention / Behandlung
Treatment-naïve newly diagnosed CIDP
Participants will receive treatment according to routine clinical practice. In Group 1, first-line treatment will usually consist of intravenous immunoglobulin (IVIg), with subsequent therapeutic decisions made by the treating neurologist according to clinical response and standard care. No investigational intervention is assigned by the study protocol.
Participants will receive treatment according to routine clinical practice. In Group 1, first-line treatment will usually consist of intravenous immunoglobulin (IVIg), with subsequent therapeutic decisions made by the treating neurologist according to clinical response and standard care. No investigational intervention is assigned by the study protocol.
Refractory CIDP
Participants with refractory CIDP will continue or receive treatments according to routine clinical practice. The study does not assign or modify treatment and is limited to observational phenotyping and biomarker analyses.
Participants with refractory CIDP will continue or receive treatments according to routine clinical practice. The study does not assign or modify treatment and is limited to observational phenotyping and biomarker analyses.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Clinical response status to first-line intravenous immunoglobulin (IVIg) for group 1
Zeitfenster: month 3
Clinical response status at Month 3 after initiation of first-line IVIg in treatment-naïve patients with newly diagnosed chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). Response categories will be predefined and may include remission, responder, partial responder, and non-responder, based primarily on adjusted INCAT and Hand Grip Strength.
month 3

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Clinical response status
Zeitfenster: Month 6 and Month 12
Clinical response status assessed in Group 1 using predefined response categories
Month 6 and Month 12
Clinical response status - Hand Grip Strength
Zeitfenster: Month 6 and Month 12
Hand Grip Strength assessed in Group 1 using a dynamometer. measure in kg
Month 6 and Month 12
Clinical response status - Medical Research Council (MRC) Sum Score
Zeitfenster: Month 6 and Month 12
Medical Research Council (MRC) Sum Score assessed in Group 1 to evaluate global muscle strength. The total MRC score ranges from 0 to 60
Month 6 and Month 12
Clinical response status - Inflammatory Rasch-built Overall Disability Scale (I-RODS)
Zeitfenster: Months 6 and 12
Inflammatory Rasch-built Overall Disability Scale (I-RODS) score assessed in Group 1 to evaluate to evaluate activity- 24 items, score from 0 to 48
Months 6 and 12
Clinical response status - Timed Up and Go (TUG)
Zeitfenster: Month 6 and Month 12
Timed Up and Go (TUG) test performed in Group 1 to evaluate functional mobility - measure in seconds
Month 6 and Month 12
Clinical response status - Pain Visual Analog Scale (VAS)
Zeitfenster: Months 6 and 12
Pain intensity assessed in Group 1 with Visual Analog Scale (VAS) from 0 to 10
Months 6 and 12
Clinical response status - Patient Global Impression of Severity (PGI-S)
Zeitfenster: Months 6 and 12
Patient Global Impression of Severity (PGI-S) assessed in Group 1. 1-item questionnaire
Months 6 and 12
Clinical response status - Work Productivity and Activity Impairment Questionnaire: Specific Health Problem (WPAI-SHP)
Zeitfenster: Months 6 and 12
Work Productivity and Activity Impairment Questionnaire: Specific Health Problem (WPAI-SHP) score assessed in Group 1.6-items
Months 6 and 12
Association between biomarkers and ultrasound phenotypes
Zeitfenster: Baseline, Month 3, Month 6, and Month 12
statistical analysis of association of biological elements
Baseline, Month 3, Month 6, and Month 12
Association between biomarkers and clinical severity
Zeitfenster: Baseline, Month 3, Month 6, and Month 12
statistical analysis of association of biological and clinical elements
Baseline, Month 3, Month 6, and Month 12
Association between biomarkers and refractory disease
Zeitfenster: Baseline, Month 3, Month 6, and Month 12
statistical analysis of association of biological elements
Baseline, Month 3, Month 6, and Month 12

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. September 2026

Primärer Abschluss (Geschätzt)

31. Dezember 2028

Studienabschluss (Geschätzt)

30. September 2029

Studienanmeldedaten

Zuerst eingereicht

17. Juli 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

17. Juli 2026

Zuerst gepostet (Tatsächlich)

22. Juli 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

22. Juli 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

17. Juli 2026

Zuletzt verifiziert

1. Juli 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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