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CompletedNCT01642225

Desensitization Protocol for Deceased Donor List

Status
Completed
Phase
Study type
Observational
Enrollment
180 (actual)
Sponsor
University of Miami · Academic / Other
Sex
All
Age
7 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Purpose of the study: The specific aims of this study are to evaluate overall efficacy and safety of the pre-transplant IVIG treatment in our transplant center since 2007 and to identify factors affecting treatment outcomes in order to improve patient selection and treatment protocols for future patients.

Detailed description

Background: Intravenous immunoglobulin (IVIG) infusion is one of several novel approaches to decrease antibody levels for highly sensitized kidney transplant candidates \[1, 2\]. This approach can potentially give a chance of kidney transplantation to end-stage renal failure patients who could never receive transplantation because of high levels of antibodies and persistent positive crossmatches to all potential kidney donors. Many transplant centers have used this strategy in order to increase transplant rates of highly sensitized patients with various levels of anti-HLA antibodies. However, the responses to the treatment seem to be different in each patient and factors affecting treatment outcome have yet to be determined.

Conditions

Timeline

Start date
2012-06-01
Primary completion
2014-06-01
Completion
2014-06-01
First posted
2012-07-17
Last updated
2014-10-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01642225. Inclusion in this directory is not an endorsement.

Desensitization Protocol for Deceased Donor List (NCT01642225) · Clinical Trials Directory