Clinical Trials Directory

Trials / Completed

CompletedNCT00231439

Post-Poliosyndrome Treated With Intravenous Immunoglobulin (IvIg)

Post-Polio Syndrome Treated With Intravenous Immunoglobulin (IvIg)

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
40 (planned)
Sponsor
Haukeland University Hospital · Academic / Other
Sex
All
Age
0 Years – 75 Months
Healthy volunteers
Accepted

Summary

Inflammatory cytokines in the cerebrospinal fluid may contribute to the new muscle weakness, fatigue and pain experienced by patients with post-polio syndrome. Intravenousimmunoglobulin (IvIg) reduces this inflammation. The purpose of this study is to investigate the clinical effect of IvIg in post-polio syndrome.

Detailed description

Post-polio syndrome (PPS) is characterised by new muscle weakness, pain, and fatigue several years after the attack of acute polio. This leads to increased disability, and up to now only supportive therapy is available. Patients with PPS lose more motor neurons than expected and surviving neurons fail to maintain neurogenic supply to enlarged motor units. New data report an increased level of inflammatory cytokines in the cerebrospinal fluid (CSF). Immune modulating therapy like IvIg could be an option and this pilot study is the first to investigate the clinical effect of IvIg in PPS. In addition, levels of cytokines in CSF and serum before and after treatment will be investigated.

Conditions

Interventions

TypeNameDescription
DRUGIvIg

Timeline

Start date
2003-08-01
Completion
2004-07-01
First posted
2005-10-04
Last updated
2005-12-13

Source: ClinicalTrials.gov record NCT00231439. Inclusion in this directory is not an endorsement.