NCT07431814

Brief Summary

The overall objective of compiling this registry is to obtain a complete collection of data, in a dedicated database, on all patients who have undergone transplantation at our Center in order to assess the main causes of mortality, hospitalization, and morbidity.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jun 2018

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 28, 2018

Completed
5.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 29, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 29, 2023

Completed
1.9 years until next milestone

First Submitted

Initial submission to the registry

December 5, 2025

Completed
3 months until next milestone

First Posted

Study publicly available on registry

February 25, 2026

Completed
Last Updated

February 25, 2026

Status Verified

December 1, 2025

Enrollment Period

5.5 years

First QC Date

December 5, 2025

Last Update Submit

February 20, 2026

Conditions

Heart Transplant

Keywords

heart transplant

Outcome Measures

Primary Outcomes (1)

  • Overall Mortality in Heart Transplant Recipients

    The primary objective of this registry is to evaluate overall mortality of the cohort of heart transplanted patients at Fondazione IRCCS Policlinico San Matteo.

    After 1 month, 6 months, one year, and 5 years

Secondary Outcomes (1)

  • Cause-Specific Mortality, Morbidity, and Hospitalization

    After 1 month, 6 months, one year, and 5 years

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

The objective of the registry is to have an up-to-date, high quality and exhaustive data collection for the evaluation of the overall survival in the population of heart transplanted recipients and the incidence of hearth, kidney, infectious complications over the last thirty years and their determinants.

You may qualify if:

  • To be included in the study the patient must:
  • Give written informed consent to participate for the prospective evaluations
  • Be a heart transplanted patient
  • Be aged 18 years and over

You may not qualify if:

  • Withdrawn of the consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Fondazione IRCCS Policlinico San Matteo

Pavia, 27100, Italy

Location

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
5 Years
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principal investigator

Study Record Dates

First Submitted

December 5, 2025

First Posted

February 25, 2026

Study Start

June 28, 2018

Primary Completion

December 29, 2023

Study Completion

December 29, 2023

Last Updated

February 25, 2026

Record last verified: 2025-12

Locations

IT(1)