Immunoglobulin Levels and Occurrence of Infections After Lung Transplantation and Impact of IgG Replacement
NCT ID: NCT01361178
Last Updated: 2017-03-22
Study Results
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View full resultsBasic Information
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COMPLETED
NA
133 participants
INTERVENTIONAL
2011-01-31
2016-01-31
Brief Summary
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The goal of treatment of HGG in PID has been to maintain the trough IgG level above 500 mg/dl which might provide better protection against infections than do lower IgG serum concentrations. Although IgG therapy is of substantial benefit, the doses and trough levels of IgG that are optimal are not yet clearly established. The impact of high versus low IgG dosing on the frequency and severity of infections and rejection has not been studied before in LT patients with HGG. The specific aims for this study are to compare the incidence of infections in lung transplant recipients receiving higher versus lower dose of SQ IgG and to compare the incidence of infections in lung transplant recipients with mild hypogammaglobulinemia versus normal IgG levels. This study will be a single center study of all lung transplant recipients, age 18 years or older, at the University of Pittsburgh Medical Center (UPMC), with a randomized treatment arm and an observational arm.
The hypotheses for the research study are:
* Therapy with IV or SQ IgG is of substantial benefit in reducing the number of infections in lung transplant recipients with severe hypogammaglobulinemia (IgG \< 500)
* A higher dose of SQ IgG, with subsequent higher trough IgG levels, may have a higher impact on the frequency and severity of infections and rejection episodes, compared to a lower dose of SQ IgG, with subsequent lower IgG trough levels
* Lung transplant recipients with mild hypogammaglobulinemia ( IgG= 500-750) have a higher incidence of infections compared to patients with normal IgG levels
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Transplant patients who do not receive SQ IVIG
Patients participating in the observational arm of the study who do not need to receive IgG replacement.
No interventions assigned to this group
Transplant patients who receive SQ IVIG
Patients participating in the observational arm of the study who are randomized to receive a dosage of SQ IVIG due to low IgG level.
SQ IVIG
Group 1 will receive SQ IgG at the lower end of the dosing range at 100 mg/kg/week and group 2 will receive SQ IgG at the higher end of the dosing range at 200 mg/kg/week
Interventions
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SQ IVIG
Group 1 will receive SQ IgG at the lower end of the dosing range at 100 mg/kg/week and group 2 will receive SQ IgG at the higher end of the dosing range at 200 mg/kg/week
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* history of anaphylaxis to IVIG
* subjects already on IV or SQ IgG treatment
18 Years
ALL
No
Sponsors
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CSL Behring
INDUSTRY
University of Pittsburgh
OTHER
Responsible Party
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Andrej Petrov
Andrej Petrov, MD
Locations
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UPMC Comprehensive Lung Center
Pittsburgh, Pennsylvania, United States
Countries
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Other Identifiers
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09090483
Identifier Type: -
Identifier Source: org_study_id
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