CAssIOPé: Characterization of Anti-HLA Alloimmunization After Pulmonary Valve Homograft Insertion

Sponsor
Assistance Publique Hopitaux De Marseille (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06113224
Collaborator
(none)
53
2
42

Study Details

Study Description

Brief Summary

This is a prospective, monocentric, observational cohort study whose main objective is to describe the number and rate of patients who developed DSAs (Donor Specific Antibody) at 6 months post-surgery with implantation of a cryopreserved lung homograft.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Blood collection T0
  • Procedure: Blood collection 6 months
N/A

Detailed Description

Lung homograft is used in a large number of complex malformations. It is accepted that homografts may induce immune reactions in the recipient, but no immunological studies have been carried out to characterize the recipient's immune reactions to the homograft and their potential impact on valve function. In this project, the authors propose to study the immunizing character of cryopreserved lung homografts by identifying the appearance of antibodies directed against the HLA, DSA (Donor Specific Antibodies) molecules of the graft (lung homograft) at 1 month and 6 months after its surgical implantation.The primary objective will be analyzed by describing the rate of patients who developed DSA at 6 months post-surgery with implantation of a cryopreserved lung homograft.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
53 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Characterization of Anti-HLA Alloimmunization After Pulmonary Valve Homograft Insertion (CAssIOPé)
Anticipated Study Start Date :
Dec 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2026
Anticipated Study Completion Date :
Jun 1, 2027

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Control patients

Patients with an indication for cardiac surgery with extracorporeal circulation but without homograft

Procedure: Blood collection T0
2 blood samples will be taken in addition to the pre-operative check-up.

Procedure: Blood collection 6 months
1 blood sample will be taken 6 months after surgery.

Experimental: Lung homograft patients

patients requiring lung homograft implantation

Procedure: Blood collection T0
2 blood samples will be taken in addition to the pre-operative check-up.

Procedure: Blood collection 6 months
1 blood sample will be taken 6 months after surgery.

Outcome Measures

Primary Outcome Measures

  1. Detection of DSA at 6 months [6 months]

    Luminex® detection of DSA at 6 months after lung homograft implantation

Secondary Outcome Measures

  1. DSA Quantification [6 months]

    DSA will be quantified in patients who developed DSA 6 months after lung homograft implantation

  2. antibody anti-HDLA (non DSA) detection [6 months]

    Detection or non-detection of non-DSA anti-HLA antibodies will be assessed by Mean Fluorescence Intensity.

  3. Early degeneration of the homograft [6 months]

    The early degeneration of the homograft will be defined by the occurrence of at least one of the following criteria: Need to replace lung homograft Need for dilatation during catheterization of lung homografts Maximum gradient across the lung homograft ≥ 30mmhg on echography at 6 months Pulmonary insufficiency ≥ moderate on echography at 6 months

Eligibility Criteria

Criteria

Ages Eligible for Study:
14 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteriafor control patients:
  • Patient receiving a cryopreserved pulmonary valve homograft

  • Patient aged 14 or over

  • Signature of consent by adult patients/parents/guardians and assent by children

Inclusion Criteriafor patients with lung homograft :
  • Patientsreceiving a cardiac surgery with extracorporeal circulation and without lung homograft

Exclusion Criteria for both group

  • Emergency surgery patient

  • Pregnant women or childbirth within the last 6 months

  • Transfusion during the surgery or within the last 6 months

  • Patient with DSAs detected before the surgery

  • Patient with anti-HLA antibodies (non-DSAs) detected before the surgery

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Assistance Publique Hopitaux De Marseille

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Assistance Publique Hopitaux De Marseille
ClinicalTrials.gov Identifier:
NCT06113224
Other Study ID Numbers:
  • RCAPHM22_0448
First Posted:
Nov 2, 2023
Last Update Posted:
Nov 2, 2023
Last Verified:
Oct 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Nov 2, 2023