Immunologic Risk of Pregnancy in Women With Lung Transplantion : a National Multicentric Study

NCT ID: NCT05689905

Last Updated: 2024-07-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-02-27

Study Completion Date

2025-03-31

Brief Summary

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TRIGGER 1 is a previous study that evaluate the immunological risk of pregnancy in women with lung transplants in France, whose pregnancy has ended between January 1, 2012 and December 31, 2021. The primary endpoint is the occurrence of humoral rejection with a year after pregnancy.

TRIGGER 2 aims to evaluate the risk of humoral rejection if there are common antigens between the child and the lung donor. We will collect HLA typing from children to compare them to the HLA typing of the mother, the lung donor and the antibodies produced if there are.

Thus, it will help us to suggest recommendations to limit the immunological risk of pregnancy for lung transplant women.

Lung transplantation is the treatment of choice of terminal chronic respiratory failure, such as cystic fibrosis and pulmonary hypertension. Young female patient of childbearing age are concerned.

For many years, given the risk of maternal and fetal complications, pregnancies were not recommended. Studies on large cohorts of transplanted patients, particularly kidney transplanted patients, have made it possible to study the risks of maternal, obstetrical and neonatal complications.

A few studies have been published in lung transplantation on small numbers of patients. However, these publications reporting on the fate of pregnancies in cohorts of lung transplant patients do not mentioned the immunological risk, with in particular the absence of studies on the risk of humoral rejection, appearance of anti-HLA (Human Leukocyte Antigens) antibodies (Ac) and the possible appearance of anti-HLA Ac directed against the donor (donor specific antibody, DSA).

TRIGGER 1 is a previous study, whose main objective is to evaluate the immunological risk of pregnancy in women with lung transplants (mono-, bi-, or cardiopulmonary) in France, whose pregnancy has ended between January 1, 2012 and December 31, 2021. The primary endpoint is the occurrence of humoral rejection within 1 year after pregnancy.

For this study TRIGGER2, we will collect the HLA typing of the children for pregnancies that resulted in the birth of a child. Thus, we will be able to compare the HLA typing of the children with the HLA typings of the mother and the lung donor, and the antibodies produced by the mother. The primary endpoint is to evaluate the risk of humoral rejection if there are common HLA antigens between the child and the lung donor.

Detailed Description

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Conditions

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Lung Transplantation Graft Rejection Pregnancy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Common HLA antigens with the lung donor

Children who have common HLA antigens with the lung donor of their mother

HLA typing of the children

Intervention Type DIAGNOSTIC_TEST

The HLA typing is made on a mouth swab of the children, that is a painless non-invasive procedure.

No common HLA antigens with the lung donor

Children without common HLA antigens with the lung donor of their mother.

HLA typing of the children

Intervention Type DIAGNOSTIC_TEST

The HLA typing is made on a mouth swab of the children, that is a painless non-invasive procedure.

Interventions

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HLA typing of the children

The HLA typing is made on a mouth swab of the children, that is a painless non-invasive procedure.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Children born between 01/01/2012 and 31/12/2021 of female patients over 18 years old with lung transplantation (mono, uni or cardio pulmonary) in France,
* Alive at the time of our study.
* Legal guardians' consent for oral swabbing of their child and HLA typing on this swab
* Affiliated or beneficiaries of a social security system or similar

Exclusion Criteria

\- Refusal of consent by the patient and/or one of the two parents
Minimum Eligible Age

1 Year

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Institut de Recherche en Santé Respiratoire

UNKNOWN

Sponsor Role collaborator

Nantes University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Nantes University Hospital

Nantes, Loire Atlantique, France

Site Status RECRUITING

Bordeaux University Hospital

Bordeaux, , France

Site Status RECRUITING

Grenoble University Hospital

Grenoble, , France

Site Status RECRUITING

Marie Lannelongue Hospital (GHSJ)

Le Plessis-Robinson, , France

Site Status RECRUITING

Civils Hospitals Lyon

Lyon, , France

Site Status RECRUITING

AP-HM

Marseille, , France

Site Status RECRUITING

Cochin Hospital (AP-HP)

Paris, , France

Site Status RECRUITING

Strasbourg University Hospital

Strasbourg, , France

Site Status RECRUITING

Foch Hospital

Suresnes, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Isabelle DANNER-BOUCHER

Role: CONTACT

+33 2 40 16 52 67

Facility Contacts

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Isabelle DANNER-BOUCHER

Role: primary

+33 2 40 16 52 67

Angélique LECLERC

Role: backup

Julie MACEY, PH

Role: primary

33 5 57 65 63 38

Christel SAINT-RAYMOND, PH

Role: primary

33 4 76 76 75 93

Jérôme LE PAVEC, PH

Role: primary

33 1 40 94 24 30

Claire MERVEILLEUX DU VIGNAUX, PH

Role: primary

33 4 27 85 77 00

Martine-Louise REYNAUD, PU-PH

Role: primary

33 4 91 96 61 45

Pierre-régis BURGEL, PU-PH

Role: primary

33 1 58 41 21 55

Romain KESSLER, PU-PH

Role: primary

33 3 69 55 06 45

Olivier BRUGIERE, PU-PH

Role: primary

33 1 46 25 38 01

Other Identifiers

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RC22_0581

Identifier Type: -

Identifier Source: org_study_id

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