Fact CheckerSign in

NCT04356781Completed

Do IgG Level Variations in CIDP and MMN Patients Following Initial Intravenous IVIg Treatment Correlate With Ultimate Dosing

Do (IgG) Variations in Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIPD) and MMN Patients Following Initial Intravenous Immunoglobulin (IVIg) Treatment Correlate With Ultimate Dosing

Source: ClinicalTrials.gov · Last updated 17 Feb 2026

Brief summary (registry, in English)

CIDP and MMN are part of a group of chronic inflammatory conditions that affect the peripheral nervous system. In CIDP, there is chronic inflammation of the peripheral nerves and nerve roots leading to demyelination. The myelin sheath is vital in the rapid propagation of nerve impulses between the central nervous system and the peripheral sensory receptors and muscles. By definition CIDP must progress over 8 or more weeks and can either have a slowly progressive disease course or a relapsing course with periods of improvement. Patients typically present with a non-length dependent neuropathy that affects motor (i.e. weakness of proximal or distal muscles, fatigue, swallowing difficulty, double vision, breathing difficulties etc) and sensory function. MMN is a similar condition to CIDP. It is an autoimmune demyelinating neuropathy that leads to slowly progressive asymmetrical weakness that worsens over years without treatment. IVIg is a recognised treatment for CIDP and MMN. A standard starting dose of 2 g/kg/course, spread over 2-5 days, has been widely used in both research and clinical practice. Due to the chronic nature of CIDP and MMN, most patients with these conditions require repeated doses to avoid relapse, but the frequency of courses and the total dose of IVIg per course required to achieve a steady state varies between patients. Given the modest risks involved with IVIg and its cost, the lowest possible dose and frequency of administration are preferred. Current strategies to reduce dose and frequency involve assessing clinical response to lower doses, but this is both time consuming and imprecise.

Status (registry)
Completed
Study type
Observational
Enrollment
20 (actual)
First submitted
17 Apr 2020
Start date
28 Sept 2020
Primary completion date
30 Dec 2024
Lead sponsor
Walton Centre NHS Foundation Trust
NCT number
NCT04356781

What you commit to

  • Study type: Observational
  • Participants enrolled: 20
  • From 28 Sept 2020 to the primary completion date, 30 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous Intravenous immunoglobulin use in the last year
    • Age under 18
    • Lack of mental capacity to consent to treatment or to study participation
    • Concurrent treatment with steroids or other immunosuppressants

Who the study is looking for

  • Adult patients with CIDP or MMN who are starting Intravenous immunoglobulin in the Walton Centre
  • Informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The Walton Centre NHS Foundation Trust
Coordinator of this site? Confirm its status
LiverpoolUnited KingdomUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.