Evolution of Respiratory Function in Lung Transplant Patients With Moderate to Severe Covid-19 Infection

NCT ID: NCT06490744

Last Updated: 2024-07-08

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

75 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-09-04

Study Completion Date

2024-12-31

Brief Summary

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The SARS-Cov-2 infection pandemic has caused a large number of acute respiratory failures and deaths across the world. Certain factors have been identified as associated with a higher risk of developing a severe form and dying. Immunosuppression has been identified as a risk factor for progressing to a severe form.

Lung transplant patients were particularly vulnerable during this period, with a high frequency of respiratory compromise, sometimes progressing towards acute respiratory distress syndrome and, at a later stage, towards fibrotic forms. The impact of the infection on the immunological status of the patient and on the tolerance of the transplant have been little studied. The various treatments implemented during the pandemic have rapidly evolved (immunotherapy, vaccination, convalescent plasma transfusion, etc.) which may have modulated this risk. The evolution of respiratory function may be linked to the respiratory infection itself, or to the severity of respiratory damage during the infection. It is therefore relevant to compare patients with a moderate form of COVID-19 (non-intubated patients) to patients with severe forms, requiring invasive ventilation in intensive care. The evolution of respiratory function after infection has not yet been studied.

Detailed Description

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Conditions

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COVID-19 Respiratory Infection

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Adult patient
* Lung transplant patient (monopulmonary or bipulmonary)
* Covid diagnosed by RT-PCR between March 1, 2020 and December 31, 2022
* Hospitalization at the University Hospitals of Strasbourg for COVID-19
* Patient followed in the context of their lung transplant at the University Hospitals of Strasbourg
* Absence of written opposition in the subject's medical file to the reuse of their data for scientific research purposes.

Exclusion Criteria

* Subject having expressed his opposition to the reuse of his data for scientific research purposes.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Strasbourg, France

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Service d'Anesthésie Réanimation - CHU de Strasbourg - France

Strasbourg, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Charles Ambroise TACQUARD, MD

Role: CONTACT

33 3 69 55 16 08

Facility Contacts

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Charles Ambroise TACQUARD, MD

Role: primary

33 3 69 55 16 08

Other Identifiers

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9058

Identifier Type: -

Identifier Source: org_study_id

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