Immunologic Risk of Pregnancy in Women With Lung Transplantion : a National Multicentric Study
NCT ID: NCT05689905
Last Updated: 2024-07-25
Study Results
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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RECRUITING
30 participants
OBSERVATIONAL
2024-02-27
2025-03-31
Brief Summary
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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.
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Detailed Description
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Conditions
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Study Design
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COHORT
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
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
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.
Eligibility Criteria
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Inclusion Criteria
* 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
1 Year
ALL
Yes
Sponsors
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Institut de Recherche en Santé Respiratoire
UNKNOWN
Nantes University Hospital
OTHER
Responsible Party
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Locations
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Nantes University Hospital
Nantes, Loire Atlantique, France
Bordeaux University Hospital
Bordeaux, , France
Grenoble University Hospital
Grenoble, , France
Marie Lannelongue Hospital (GHSJ)
Le Plessis-Robinson, , France
Civils Hospitals Lyon
Lyon, , France
AP-HM
Marseille, , France
Cochin Hospital (AP-HP)
Paris, , France
Strasbourg University Hospital
Strasbourg, , France
Foch Hospital
Suresnes, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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RC22_0581
Identifier Type: -
Identifier Source: org_study_id
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