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UnknownNCT03172091

Volatile Organic Compounds as Markers of Acute Rejection in Lung Transplant

Analysis of Volatile Organic Compounds in the Exhaled Air Breath of in Bilateral Lung Transplant Recipients Bi-pulmonary Transplant Patients: Search for Acute Rejection Markers

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
Hopital Foch · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of research is to identify markers of acute rejection by VOC analysis in exhaled breath of bilateral-lung transplanted patients. 120 bi-lung transplanted patients will be divided into two groups : patients with acute rejection diagnosed on transbronchial biopsies and patients with no acute rejection. Exhaled breath will be collected for VOC analysis woth electronic nose and mass spectrometry. VOC profiles will be compared between the two groups of patients.

Detailed description

Prospective single-center study. A single visit, no follow-up. The visit will take place before or within five days from date of transbronchial biopsies (BTB). It will include a noninvasive collection of exhaled breath for VOC analysis. VOC analysis will be conducted using two types of devices: "electronic nose" and mass spectrometry. 200 bi-lung transplanted patients will be enrolled and divided into two groups. * Group A, Acute rejection: 100 patients. Diagnosis of acute rejection retained on transbronchial biopsies or functional anomalies with the necessity of modifying the immunosuppressive regimen. * Group B, control: 100 patients. Patients without respiratory functional abnormality and normal transbronchial biopsy. VOC, detected by electronic nose and identified by mass spectrometry, will be compared between patients with a confirmed diagnosis of acute rejection (group A) and patients without rejection (control group B) The duration of participation of each patient is 1 day. The duration of the inclusion period is estimated at 54 months from the first inclusion. The expected total duration of the research is 54 months

Conditions

Interventions

TypeNameDescription
DEVICEeNose (electronic nose)Collection of exhaled breath for an immediate analysis by electronic nose
DEVICESpectrometryCollection of exhaled breath for an immediate analysis by mass spectrometry

Timeline

Start date
2017-06-27
Primary completion
2021-10-01
Completion
2021-10-01
First posted
2017-06-01
Last updated
2021-04-26

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT03172091. Inclusion in this directory is not an endorsement.