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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04973943
Other study ID # FreeDNA-CAR
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 19, 2019
Est. completion date April 2022

Study information

Verified date July 2021
Source Puerta de Hierro University Hospital
Contact Marta B Jimenez-Blanco Bravo, MD
Phone 0034 637747916
Email martajbb@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

FreeDNA-CAR is a prospective, observational multicenter study, that will include a total of 200 adult heart transplant (HT) patients from 14 centers in Spain. Our main objective is to test donor-derived Cell-Free DNA (dd-cfDNA) against endomyocardial biopsy (EMB) for the diagnosis of acute cellular rejection.


Description:

All patients will be enrolled immediately after HT, and will undergo undergo routine surveillance EMB at 15 days, 1 month, 2, 3, 4, 6 and 12 months after HT. Simultaneously with each EMB, dd-cfDNA will be measured in plasma.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date April 2022
Est. primary completion date April 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients > 18 years old who undergo heart transplant during the recruiting period Exclusion Criteria: - Patients with moderate or severe Primary Graft Dysfunction - Patients on invasive mechanical ventilation 15 days after heart transplant - Patients on renal replacement therapy, continuous or periodic, 15 days after heart transplant - Heart Transplant due to a cardiomyopathy that could potentially recur on the graft (cardiac amyloidosis, Chagas disease or sarcoidosis, amongst others) - Multiorgan transplant

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Donor-derived cell Free DNA
Measurement of dd-cfDNA and comparison against grade of rejection as determined by endomyocardial biopsy, taken simultaneously

Locations

Country Name City State
Spain Hospital Universitario A Coruña A Coruña
Spain Hospital Bellvitge Barcelona
Spain Hospital Clinic de Barcelona Barcelona
Spain Hospital Santa Creu i Sant Pau Barcelona
Spain Hospital 12 octubre Madrid
Spain Hospital Universitario Gregorio Marañón Madrid
Spain University Hospital Puerta de Hierro Majadahonda Madrid
Spain Hospital Virgen de la Arrixaca Murcia
Spain Hospital Universitario Central de Asturias Oviedo Asturias
Spain Clinica Universitaria de Navarra Pamplona Navarra
Spain Hospital Virgen del Rocio Sevilla
Spain Hospital La Fe Valencia

Sponsors (1)

Lead Sponsor Collaborator
Puerta de Hierro University Hospital

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Association between dd-cfDNA levels and the presence of acute cellular rejection Association between dd-cfDNA levels above a certain cut-point and the presence of treatable acute cellular rejection as determined by endomyocardial biopsy (graded by International Society of Heart and Lung Transplantation 2010 classification, grade > 1R). 1 year
Secondary Area under curve for dd-cfDNA To define a cutt-off point of dd-cfDNA level with a high negative predictive value that could obviate the need to perform surveillance endomyocardial biopsies 1 year
Secondary Correlation between dd-cfDNA and antibody mediated rejection (AMR) Correlation between dd-cfDNA and antibody mediated rejection (AMR) 1 year
Secondary Association between dd-cfDNA and immunosuppressive (IS) treatment Subanalysis of association between dd-cfDNA and rejection stratified by IS regimen (type and dose of drug). 1 year
Secondary Association between dd-cfDNA (%) and left ventricular ejection fraction Association between dd-cfDNA and left ventricular ejection fraction (LVEF). All echocardiograms will be performed on the same day of EMB. 1 year
Secondary Determine the biomarker's kinetics at 15 days post-transplant Determine dd-cfDNA levels at 15 days post-transplant in absence of rejection 15 days
Secondary Association between dd-cfDNA levels and cytomegalovirus (CMV) infection Association between dd-cfDNA levels and CMV infection as determined by CMV polymerase chain reaction (number of copies per ml) 1 year
Secondary Determine a cut-off point of dd-cfDNA that allows to differentiate between acute cellular rejection (ACR) and antibody mediated rejection (AMR) Determine a cut-off point of dd-cfDNA that allows to differentiate between acute cellular rejection (ACR) and antibody mediated rejection (AMR) 1 year
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