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Use of Atorvastatin (Lipitor) to Decrease Panel Reactive Antibody Titers

Primary Purpose

End-Stage Kidney Disease

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Atorvastatin (Lipitor)
Sponsored by
University of Chicago
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for End-Stage Kidney Disease focused on measuring Kidney Disease, Lipitor, Atorvastatin, Allosensitization

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Eighteen years or older, On the waiting list for a kidney transplant list On hemodialysis or peritoneal dialysis Exclusion Criteria: Pregnant woman Patients who need ongoing blood products Patients with failed organs having active rejection Other therapies to decrease PRA Patients listed for multi-organ transplants (other than kidney-pancreas)

Sites / Locations

  • The University of Chicago

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Lipitor

Arm Description

Outcomes

Primary Outcome Measures

This study is to identify subjects who are highly sensitized with these antibodies, and treat them in such a way, that it may become possible to transplant kidneys into them.

Secondary Outcome Measures

Full Information

First Posted
September 1, 2005
Last Updated
January 9, 2013
Sponsor
University of Chicago
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1. Study Identification

Unique Protocol Identification Number
NCT00143741
Brief Title
Use of Atorvastatin (Lipitor) to Decrease Panel Reactive Antibody Titers
Official Title
Use of Atorvastatin (Lipitor) to Decrease Panel Reactive Antibody Titers
Study Type
Interventional

2. Study Status

Record Verification Date
January 2013
Overall Recruitment Status
Completed
Study Start Date
May 2005 (undefined)
Primary Completion Date
December 2010 (Actual)
Study Completion Date
July 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Chicago

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to identify subjects who are highly sensitized with antibodies. It is difficult for these patients to find suitable kidneys. We propose to treat such patients to decrease the antibodies in such a way, that it may become possible to safely transplant kidneys into them.
Detailed Description
Kidney transplantation is the desired treatment of choice in subjects with end-stage kidney disease (ESRD). The average waiting time for subjects to receive a "deceased donor" kidney transplant is 3-5 years. Currently, there are about 60,000 subjects on the national waiting list, and about 13,000-14,000 kidney transplants are performed each year. Approximately, 25% of subjects on the waiting list are "highly sensitized", meaning that they have natural proteins (antibodies) that aggressively protect their bodies from the invasion of foreign proteins. These individuals often have a difficult time accepting transplanted kidneys. The purpose of this study is to identify subjects who are highly sensitized with these antibodies, and treat them in such a way, that it may become possible to transplant kidneys into them. Drugs like atorvastatin (Lipitor) may decrease the levels of these anti-bodies and increase the possibility of these subjects to receive a kidney transplant. This research study is being done because currently, there are very limited and cumbersome treatment options to address this issue, subjects who are highly sensitized with antibodies, may unfortunately wait for a very long time or may never get transplanted.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End-Stage Kidney Disease
Keywords
Kidney Disease, Lipitor, Atorvastatin, Allosensitization

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Lipitor
Arm Type
Other
Intervention Type
Drug
Intervention Name(s)
Atorvastatin (Lipitor)
Intervention Description
20mg every day, taken by mouth. Dose could be increased up to 60mg every day during the course of the trial if tests indicate this is needed.
Primary Outcome Measure Information:
Title
This study is to identify subjects who are highly sensitized with these antibodies, and treat them in such a way, that it may become possible to transplant kidneys into them.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Eighteen years or older, On the waiting list for a kidney transplant list On hemodialysis or peritoneal dialysis Exclusion Criteria: Pregnant woman Patients who need ongoing blood products Patients with failed organs having active rejection Other therapies to decrease PRA Patients listed for multi-organ transplants (other than kidney-pancreas)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pradeep Kadambi, MD
Organizational Affiliation
The University of Chicago, 5841 South Maryland Ave., MC 5100 Chicago, IL 60637
Official's Role
Principal Investigator
Facility Information:
Facility Name
The University of Chicago
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60637
Country
United States

12. IPD Sharing Statement

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Use of Atorvastatin (Lipitor) to Decrease Panel Reactive Antibody Titers

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