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Clinical and Immunological Outcomes of Living and Deceased Donor Transplantation (TxBo2022)

S

Scientific Institute for Research Hospitalization and Healthcare (IRCCS)

Status

Enrolling

Conditions

Transplant Recipient (Kidney)

Study type

Observational

Funder types

Other

Identifiers

NCT06759831
TxBo2022

Details and patient eligibility

About

This is a retrospective, prospective, single-centre, non-pharmacological observational study.

The primary objective is to investigate the long-term prognosis of the kidney transplant function of different types of donors.

Full description

It provides for the systematic collection of clinical information of patients undergoing kidney transplantation from 01/01/2017 until the Ethics Committee approves the study and the Director General of the IRCCS issues the authorisation. Data collection will continue for 9 years after the start of the study.

Patients participating in the prospective part will be treated according to clinical practice, in accordance with the judgement of the physician and the information reported in the Technical Data Sheet of each individual product of any concomitant therapies administered according to clinical practice. There are no additional study-specific visits/examinations for enrolled patients and any data recorded for the purposes of the study is collected for care purposes during the patient's normal course of treatment.

Enrollment

1,293 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥ 18 years.
  • Kidney transplant recipient from any donor.
  • Acquisition of Informed Consent to study participation and data processing.

Exclusion criteria

Trial contacts and locations

1

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Central trial contact

Gaetano La Manna, MD; Giorgia Comai, MD

Data sourced from clinicaltrials.gov

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