Skip to main content
OpenTrials
Completed

NCT Number: NCT01642225

Desensitization Protocol for Deceased Donor List

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

7 year–75 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Miami

Miami, Florida, 33136, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Recent (< 3 months) high levels of anti-HLA antibodies (at least one cPRA ≥ 40%).
  • Waiting time greater than 1 year for blood type AB, 2 years for blood types A, B, or O.

Exclusion criteria

  • Female subject is pregnant or lactating.
  • Subject has an uncontrolled concomitant infection or any other unstable medical condition (e.g., uncontrolled cardiovascular disease) that could interfere with the study objectives.
  • Subject has an uncontrolled active hepatitis B, hepatitis C, or HIV infection.
  • Subject has a current malignancy or a recent history of any malignancy that is deemed to be contraindicated to kidney transplantation.
  • Subject has a psychiatric illness that, in the judgment of caring physicians, may interfere with study participation.

Treatment and study plan

Primary outcomes

  1. Anti HLA antibody level

    Time frame: after IVIG infusion

Secondary outcomes

  1. Number of patients transplanted

    Time frame: at the end of study

Sponsors and collaborators

Lead sponsor

University of Miami

Other

Registry information

Important dates

Study start
2012
Primary completion
2014
Study completion
2014
First posted
Jul 17, 2012
Registry last updated
Oct 20, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.