Actively Recruiting

Age: 18Years +
All Genders
ID06759831

Clinical and Immunological Outcomes of Kidney Transplantation Comparing Living and Deceased Donor Types in an Observational Study

Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2025-01-06

1293

Participants Needed

1

Research Sites

465 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research focuses on patients who have received kidney transplants, aiming to study the long-term outcomes and kidney function after transplantation from various types of donors. It is a retrospective and prospective observational study conducted at a single center without the use of drugs. The main goal is to understand how kidney transplants perform over extended periods depending on the donor type. The study involves systematically collecting clinical information from patients who have undergone kidney transplantation starting from January 1, 2017, and continuing until the Ethics Committee approves the study and the institution's director authorizes it. Data collection will proceed for nine years from the study's start. Patients in the prospective part receive treatment based on standard clinical practice, guided by their doctor's judgment and product information for any therapies used. There are no extra study visits or exams beyond routine care. Participants will be followed as part of their regular treatment, with all data collected during usual medical visits. Researchers will monitor kidney transplant function at various time points, including 1 month, 6 months, 1 year, 5 years, and 10 years after transplantation. This approach ensures the study measures long-term transplant outcomes without altering patient care or adding study-specific procedures.

CONDITIONS

Official Title

Clinical and Immunological Outcomes of Living and Deceased Donor Transplantation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 2425 18 years.
  • Kidney transplant recipient from any donor.
  • Acquisition of Informed Consent to study participation and data processing.
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Trial Site Locations

Total: 1 location

1

IRCCS Sant'Orsola University Hospital - Nephrology, Dialysis and Transplant Unit

Bologna, BO, Italy, 40138

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Research Team

G

Giorgia Comai, MD

G

Gaetano La Manna, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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