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RECRUITING
NCT06112951
NA

A Prospective Randomized Trial of ECP in Subclinical AMR

Sponsor: Medical University of Vienna

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to evaluate the therapeutic effect of extracorporeal photopheresis in subclinical antibody-mediated rejection after lung transplantation.The main questions it aims to answer are: 1. Does ECP therapy result in a significant reduction in MFI (Mean Fluorescence Intensity) from the baseline MFI in clinically stable patients with persistent (\>6 months) dnDSAs (MFI\>1000)? 2. What is the impact of ECP therapy on the following outcomes in these patients: ACR, clinical AMR, CLAD, infections, drop-out rate, survival, adverse events? Participants will be randomized into two groups. Each group will include 40 patients. The control group will be observed and no active treatment will be administered. The treatment group will receive extracorporeal photopheresis. First, a two-day treatment cycle will be performed once every second week for the first two months. Then, a two-day treatment cycle will be performed once a month for 6 months. Researchers will compare the two groups regarding: MFI value, development of ACR, clinical AMR, CLAD, infections, survival, adverse events, immunophenotyping, miRNA expression profiling, cytokine expression, gene expression signature of PBMCs and proteomic characterization.

Official title: The Use of Extracorporeal Photopheresis as Immunomodulatory Therapy of Subclinical Antibody-mediated Rejection After Lung Transplantation: a Prospective RCT

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2024-03-01

Completion Date

2027-06-01

Last Updated

2024-07-09

Healthy Volunteers

No

Interventions

PROCEDURE

Extracorporeal Photopheresis

Patients randomized into the interventional group will receive ECP. ECP will be started within one week after randomization. Initially a two-day treatment cycle will be performed once every second week for the first two months. Then, a two-day treatment cycle will be performed once a month for 6 months.

Locations (7)

Medical University of Vienna

Vienna, Austria

UZ Leuven

Leuven, Belgium

University Hospital Center Zagreb

Zagreb, Croatia

Copenhagen University Hospital, Rigshospitalet

Copenhagen, Denmark

Hôpital Foch

Suresnes, France

Policlinico San Matteo Pavia Fondazione IRCCS

Pavia, Italy

University Medical Centre Ljubljana

Ljubljana, Slovenia