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The Paired Donation Consortium Paired Donation Program

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT00374400
Recruitment Status : Completed
First Posted : September 11, 2006
Last Update Posted : January 3, 2008
Sponsor:
Collaborator:
The Paired Donation Consortium
Information provided by:
University of Cincinnati

Tracking Information
First Submitted Date September 8, 2006
First Posted Date September 11, 2006
Last Update Posted Date January 3, 2008
Study Start Date September 2004
Primary Completion Date Not Provided
Current Primary Outcome Measures Not Provided
Original Primary Outcome Measures Not Provided
Change History
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title The Paired Donation Consortium Paired Donation Program
Official Title The Paired Donation Consortium Paired Donation Program
Brief Summary The purpose of the protocol is to increase the number of living donor transplants by eliminating immune incompatibilities between donors and recipients through paired donation.
Detailed Description

The purpose of the protocol is to increase the number of living donor transplants by eliminating immune incompatibilities between donors and recipients through paired donation.

To increase the number of patients transplanted by paired donation by establishment of regional paired donation programs.

To develop educational programs for potential living donors and their recipient, as well as the opportunity for transplant professionals to increase acceptance of the PDC to maximize the opportunity for organ donation.

To identify and evaluate ethical and psychological factors that may influence the effects of paired donation on living kidney donation.

Study Type Observational
Study Design Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Not Provided
Study Population Not Provided
Condition Kidney Transplant
Intervention Not Provided
Study Groups/Cohorts Not Provided
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Completed
Estimated Enrollment
 (submitted: September¬†8,¬†2006)
100
Original Enrollment Same as current
Actual Study Completion Date November 2007
Primary Completion Date Not Provided
Eligibility Criteria

Inclusion Criteria:

  • Persons capable of providing written informed consent.
  • Each recipient must have one or more medically suitable donors who are either ABO-incompatible or HLA-incompatible.

Exclusion Criteria:

  • Persons with eligible, compatible donor.
Sex/Gender
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers Yes
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries United States
Removed Location Countries  
 
Administrative Information
NCT Number NCT00374400
Other Study ID Numbers PDC
Has Data Monitoring Committee Not Provided
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party Not Provided
Study Sponsor University of Cincinnati
Collaborators The Paired Donation Consortium
Investigators
Principal Investigator: Steve Woodle, MD University of Cincinnati
PRS Account University of Cincinnati
Verification Date December 2007