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University of Minnesota Transplant Registry

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. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01062581
Recruitment Status : Recruiting
First Posted : February 4, 2010
Last Update Posted : March 29, 2022
Sponsor:
Information provided by (Responsible Party):
University of Minnesota

Brief Summary:
Under Transplant Information Services (TIS), the University of Minnesota Transplant Registry (UMTR) will serve as the repository for core research data.

Condition or disease
Transplant Recipient Transplant Donation

Detailed Description:
UMTR is a system of ongoing registration of cases seen in the transplant program at the University of Minnesota. The registry will: (1) provide core outcomes data and background information necessary to conduct outcomes management research in solid organ transplantation and advanced lung disease, and (2) support cutting edge research through existing program specific databases in liver, intestine, pancreas, islet, kidney, heart and lung transplantation.

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Study Type : Observational
Estimated Enrollment : 10000 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: University of Minnesota Transplant Registry
Study Start Date : March 1997
Estimated Primary Completion Date : January 2050
Estimated Study Completion Date : January 2050

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Organ Donation

Group/Cohort
Transplant Recipients and Living Donors

All transplant recipients receiving transplants at the University of Minnesota (kidney, pancreas, liver, heart, lung, islet, intestine). All ages.

All living donors donating an organ at the University of Minnesota (kidney, pancreas, liver, lung) (by law, living donors are required to be at least 18 years old)





Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
University of Minnesota Transplant Center University of Minnesota Medical Center, Fairview
Criteria

Inclusion Criteria:

  • Received a transplanted organ at the University of Minnesota
  • Living donor who donates an organ at the University of Minnesota

Exclusion Criteria:

  • Did not receive a transplant at the University of Minnesota
  • Did not donate an organ at the University of Minnesota

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01062581


Contacts
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Contact: Chris Schoenecker, AA 612-625-8612 schoe008@umn.edu

Locations
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United States, Minnesota
University of Minnesota Transplant Information Services Recruiting
Minneapolis, Minnesota, United States, 55414
Contact: Kathryn S Long, RN    612-625-0607    klong1@fairview.org   
Sponsors and Collaborators
University of Minnesota
Investigators
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Principal Investigator: Arthur Matas, MD University of Minnesota
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Responsible Party: University of Minnesota
ClinicalTrials.gov Identifier: NCT01062581    
Other Study ID Numbers: 0704M05324
First Posted: February 4, 2010    Key Record Dates
Last Update Posted: March 29, 2022
Last Verified: March 2022
Keywords provided by University of Minnesota:
Recipient
Donor
Organ Transplant
Registry
University of Minnesota