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Study of CIDP Patients During IVIG Treatment

This study has been completed.

Sponsored by: University of Aarhus
Information provided by: University of Aarhus
ClinicalTrials.gov Identifier: NCT00305266
  Purpose

The aim of this study is to quantify the effect of IVIG treatment in a group of patients with chronic inflammatory demyelinating polyradiculoneuropathy(CIDP), who requires continues treatment of IVIG at regular intervals of 3-10 weeks:

  1. During continues treatment of IVIG at regular intervals of 3-10 weeks.
  2. During pause in treatment.

Hypothesis:

  1. The disease activity in the patients are cyclical correlating to the treatment intervals.
  2. Pause in treatment will increase disease activity, which can be quantified with symptom scores, disability scales, and clinical test.

Primary effect parameter is muscle strength quantified by isokinetic dynamometry.

Added to the protocol there is an immunological study of inflammatory markers in blood samples of patients under treatment pause.


Condition Intervention
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
Drug: intravenous gammaglobulin

Genetics Home Reference related topics:   Autoimmune Diseases   Neurologic Diseases   Peripheral Nerve Disorders  

ChemIDplus related topics:   Globulin, Immune   Immunoglobulins  

U.S. FDA Resources

Study Type:   Observational
Study Design:   Prospective
Official Title:   "Clinical Study of Intravenous Immunoglobulin Treatment of Patients With Chronic Inflammatory Demyelinating Polyradiculoneuropathy"

Further study details as provided by University of Aarhus:

Enrollment:   11
Study Start Date:   August 2005
Study Completion Date:   August 2007

Intervention Details:
    Drug: intravenous gammaglobulin
    individual dose
Detailed Description:

Background: Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a rare autoimmune disease of the peripheral nervous system characterized by demyelination of the nerves, which causes muscle weakness and sensory loss. Treatment is immune modulating, and intravenous immunoglobulin (IVIG) is first line therapy.Several trials have demonstrated effect on motor function by the initial treatment, but the effect of consecutive IVIG treatment is only sporadic described in the literature.

It is a clinical study including present CIDP patients in treatment at the University Hospital of Aarhus. The patients will be evaluated several times before and after IVIG treatment, to describe the effect profile.

The primary effect parameter is muscle strength quantified by isokinetic dynamometry at ankle knee, hip, wrist, elbow and shoulder. That is a sensitive method of measuring the strength of the larger muscle groups, correlating with symptoms and signs of neuropathy.

Severity of neuropathy among the patients will also be described applying nerve conduction studies, quantitative sensory testing of threshold for detecting vibration and cold at upper and lower limbs, the Neuropathy Disability Scale, the Neuropathy Symptom Score,the overall disability sum score, 9 hole peg test, walking test, and the Short-form 36 health questionnaire.

Added to the protocol there is an immunological study of inflammatory markers in blood samples of patients under treatment pause.

Objective:

With this study we will describe some important aspects in the immune response causing the inflammatory lesions in CIDP and MMN, including:

  1. Recruitment of immune cells to the affected tissue by chemoattraction. (Chemokine receptors on mononuclear cells)
  2. Crossing the blood-nerve barrier: interactions and adhesion between the lymphocyte and endothelial cell, transendothelial diapedesis and enzymatic degeneration of the basal lamina.(Adhesion molecules on mononuclear cells and soluble in plasma, metalloproteinases)
  3. Synthesis of mRNA and secretion of regulatory cytokines.
  Eligibility
Ages Eligible for Study:   18 Years to 80 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria:

  • Motor and sensory dysfunction involving more than one limb.
  • Electrodiagnostic study with signs of demyelination

Exclusion Criteria:

  • Prior systemic allergic reaction to IVIG
  • Severe systemic disease
  • Other conditions associated with neuropathy (eg diabetes, lack of vitamin- B12)
  • Pregnancy
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00305266

Locations
Denmark
Aarhus University Hospital, Department of Neurology    
      Aarhus, Denmark

Sponsors and Collaborators
University of Aarhus

Investigators
Principal Investigator:     Henning Andersen, MD     Aarhus University Hospital    
Study Chair:     Johannes Jakobsen, professor     Aarhus University Hospital    
  More Information

Study ID Numbers:   2005-0018, EudraCT nr.: 2004-004357-26
First Received:   March 20, 2006
Last Updated:   November 30, 2007
ClinicalTrials.gov Identifier:   NCT00305266
Health Authority:   Denmark: Danish Medicines Agency

Keywords provided by University of Aarhus:
CIDP  
IVIG  
gammaglobulin  
Chronic Inflammatory Demyelinating Polyradiculoneuropathy  

Study placed in the following topic categories:
Autoimmune Diseases
Gamma-Globulins
Demyelinating Diseases
Polyradiculoneuropathy
Polyneuropathies
Demyelinating diseases
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
Neuromuscular Diseases
Immunoglobulins, Intravenous
Peripheral Nervous System Diseases
Rho(D) Immune Globulin
Autoimmune Diseases of the Nervous System
Immunoglobulins

Additional relevant MeSH terms:
Immunologic Factors
Immune System Diseases
Physiological Effects of Drugs
Nervous System Diseases
Pharmacologic Actions

ClinicalTrials.gov processed this record on July 03, 2008




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