Randomized Open-label Trial to Compare Efficacy and Tolerance of Corticosteroids and IVIg

Phase 3

Completed

• Conditions: Demyelinating Polyneuropathy
• Interventions: Drug: Immunoglobulin perfusion; Drug: Prednisone

• Registration Number: NCT01349270
• Lead Sponsor: Centre Hospitalier Universitaire de Saint Etienne

Brief Summary

Treatment of Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) is a challenge because disease may generate important disability in patients including young adults. Randomized trials showed that corticosteroids, plasma exchanges and intravenous immunoglobulin (IVIg) can reduce impairment on a short term period but the treatment of a chronic disease doesn't agree with it. Corticosteroids and IVIg are the first line CIDP treatments. No study permits to demonstrate the superiority of one treatment to the other. Long term adverse effects of corticosteroids and IVIg cost are the respective limitation of their use. The investigators scheduled to recruit 40 CIDP patients in 23 French centres to receive either 0,8mg/kg/day of prednisone progressively tapered over 6 months or a monthly 2g/kg cure of IVIg during 6 months. Patients will be followed during 6 months after the treatment.

Detailed Description

Not available

Basic Information
|
Recruitment & Eligibility
|
Study & Design
|
Trial Locations

Study Timeline

• Study Start: 2004-06
• Study First Submitted: 2011-05-05
• Study First Submitted QC: 2011-05-05
• Study First Posted: 2011-05-06
• Primary Completion: 2013-12
• Study Completion: 2013-12
• Status Verified: 2014-09
• Last Update Submitted: 2014-09-25
• Last Update Posted: 2014-09-26

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• Man or woman between 18 and 80, Weight ≤ 100 kg,

CIDP diagnosis:

• stable or deteriorated state (no spontaneous improvement),
• with the following features:
• motor or sensory and motor deficits, and reduced or abolished tendon reflexes,
• progressive or relapsing evolution,
• global symmetric disability in more than one limb,
• disease course installation over at least 2 months,
• cerebrospinal fluid with ≤10/µL white blood cells and > 0.5 g/L protein rate (non compulsory examination),
• electrophysiological or histological signs of demyelinization,
• INCAT disability score ≥ 2 in arms or ≥ 1 in legs

Read More

Exclusion Criteria

• Severe electrophysiological axonal damage,
• Pure motor syndrome,
• Spontaneous improvement,
• Associated systemic disease that could be the cause of neuropathy,
• Severe cardiac insufficiency,
• Cardiac arrhythmia,
• Severe cardiopulmonary pathology,
• Inflammatory syndrome,
• Severe physical disease which can interfere with the trial,
• Patient in a strict salt-free diet,
• A clinically significant abnormal biological result,
• Positive serology in one of the following tests: HIV1, HIV2, A-B-C hepatitis, Hbs antigen, Lyme disease,
• IgA complete deficiency,
• History of anaphylactic reaction during previous IVIg infusion,
• Hypogammaglobulinemia (IgG < 3g/L),
• Creatinine clearance < 80 mL/min,
• Evolutive gastroduodenal ulcer, diabetes, serious infectious condition, evolutive virus disease (hepatite, herpes, varicella, zona), psychotic states not controlled by treatment, veinous or arterial thrombosis, non controlled high blood pressure, osteoporosis,
• Patient previously treated by corticosteroids, IVIg, plasma exchanges or any other immunosuppressive agent within 3 months before inclusion, except for azathioprine and mycophenolate mofetil which were tolerated in the case of the dose being unmodified within 3 months and kept unchanged during the trial,
• Experienced failure with a IVIG or prednisone prior treatment,
• Hypersensitivity to any components of the 2 treatments,
• Unsigned informed consent,
• Ongoing or planned pregnancy (mandatory pregnancy test at the screening visit), breastfeeding, effective contraception for over 3 months for women of childbearing age.

Read More

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
immunoglobulin	Immunoglobulin perfusion	patient who received monthly 2g/kg cure of intravenous Immunoglobulin during 6 months
prednisone	Prednisone	patient who received 0,8mg/kg/day of prednisone progressively tapered over 6 months

Primary Outcome Measures

Name	Time	Method
Main outcome	3 months	Rate of patients with a decreased INCAT score of at least 1 point after 3 months of treatment,; * Responders: ≥ 1 point improvement in the INCAT score at 3 months in comparison to baseline,; * Non responders: unchanged INCAT score at 3 months in comparison to baseline or patients for whom the primary endpoint can't be assessed because of the occurrence of an adverse event requiring treatment stop.

Secondary Outcome Measures

Name	Time	Method
Secondary outcome	3 months	Rate of cured patients i.e. INCAT score of 0 in legs and ≤ 1 in arms after 3, 6, 9 and 12 months,

Trial Locations

Locations (11)

CHU Grenoble; 🇫🇷 Grenoble, France

CHU Clermont-Ferrand; 🇫🇷 Clermont-Ferrand, France

Chu Marseille; 🇫🇷 Marseille, France

Chu Nancy; 🇫🇷 Nancy, France

Chu Strasbourg; 🇫🇷 Strasbourg, France

Chu Saint-Etienne; 🇫🇷 Saint-etienne, France

Chu Nantes; 🇫🇷 Nantes, France

Centre hospitalier de Valence; 🇫🇷 Valence, France

Chu Dijon; 🇫🇷 Dijon, France

CHU Nice; 🇫🇷 Nice, France

Hôpital Neurologique de Lyon; 🇫🇷 Lyon, France