Evidence map›Paper›PMID 29603842›Full record

ArticleJournal of the peripheral nervous system : JPNS2018

A randomised, multi-centre phase III study of 3 different doses of intravenous immunoglobulin 10% in patients with chronic inflammatory demyelinating polyradiculoneuropathy (ProCID trial): Study design and protocol.

David R Cornblath, Hans-Peter Hartung, Hans D Katzberg, Ingemar S J Merkies, Pieter A van Doorn

Open access · hybridAbstract read
In one paragraph

Article in Journal of the peripheral nervous system : JPNS, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
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  4. Review
  5. iSTAND trial of IVIG in POTS: a step in the right direction, but more studies are needed.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2025
    Article
  6. Review
  7. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 5 institutions in 4 countries.

David R CornblathDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Hans-Peter HartungDepartment of Neurology, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Hans D KatzbergDepartment of Neurology, University of Toronto, Toronto General Hospital/UHN, Toronto, Ontario, Canada.
Ingemar S J MerkiesDepartment of Neurology, Maastricht University Medical Center, Maastricht, The Netherlands.
Pieter A van DoornDepartment of Neurology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Erasmus MC · NLHeinrich Heine University Düsseldorf · DEJohns Hopkins University · USMaastricht University · NLToronto General Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) show varying degrees of response to intravenous immunoglobulin (IVIg) therapy. This randomised phase III study in patients with CIDP (ProCID trial) will compare the efficacy and safety of 3 different doses (0.5, 1.0, and 2.0 g/kg) of IVIg 10% (panzyga) administered every 3 weeks for 24 weeks. The primary efficacy endpoint is the rate of treatment response, defined as a decrease in adjusted inflammatory neuropathy cause and treatment disability score of ≥1 point, in the IVIg 1.0 g/kg arm at week 24. Patients with definite or probable CIDP according to European Federation of Neurological Sciences/Peripheral Nerve Society criteria with IVIg or corticosteroid dependency and active disease are eligible. All potentially eligible patients will undergo IVIg or corticosteroid dose reduction (washout phase) over ≤12 weeks or until deterioration of CIDP (active disease). Patients with deterioration during the washout phase will be randomised to receive study treatment during a dose-evaluation phase starting with a loading dose of IVIg 2.0 g/kg followed by maintenance treatment with IVIg 0.5, 1.0, or 2.0 g/kg every 3 weeks. Rescue medication (2 doses of IVIg 2.0 g/kg given 3 weeks apart) will be administered to patients in the IVIg 0.5 and 1.0 g/kg groups who deteriorate after week 3 and before week 18 or who do not improve at week 6. Safety, tolerability and quality of life will be assessed. The ProCID study will provide new information on the best maintenance dose of IVIg for patients with CIDP.

Indexed as

Immunoglobulins, IntravenousPolyradiculoneuropathy, Chronic Inflammatory DemyelinatingClinical Trials, Phase III as TopicDisability EvaluationDose-Response Relationship, DrugDouble-Blind MethodFemaleHumansMaleMulticenter Studies as TopicQuality of LifeRandomized Controlled Trials as TopicResearch DesignTreatment OutcomeImmunoglobulins, Intravenouschronic inflammatory demyelinating polyradiculoneuropathyintravenous immunoglobulinrandomised-controlled trialstudy designtrial protocol

Identifiers

PMID29603842
PMCPMC6033152
OpenAlexW2795095949

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.