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Clinical Trial Summary

The aim of this study was to evaluate the diagnostic yield for lung complication after allo-HSCT by multiple parameter system through BAL.


Clinical Trial Description

一) Adult patients with hematology disease under allo-HSCT at any phase of treatment are enrolled according to the following criteria:

1. lung infiltration detection at computed tomography (CT) scan.

2. Patients with fever, cough, respiratory symptoms. According to the investigators, the patients fulfilling these criteria undergo BAL as soon as possible

二) The BALF samples were tested using such methods

1. classic microbiological cultures designed for bacteria, fungi, and mycobacteria.

2. Detection of human cytomegalovirus (CMV) and EB virus in serum and BAL was tested using a Real-time PCR kit.

3. Detection of aspergillus galactomannan antigen 1,3-beta-D-glucan in serum and BAL was performed using an enzyme immunoassay method.

4. Cytological and pathogenic microscopic evaluation in BALF

5. Flow cytological analysis of T lymphocyte subsets in BALF and serum

6. Cytokine detection in BALF and serum

7. Microbiology detection in BALF by mNGS

三) Pathogenic spectrum analysis and Targeted etiological therapy ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04051372
Study type Observational [Patient Registry]
Source Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Contact xianmin song, M.D.
Phone 86-21-37798987
Email shongxm@139.com
Status Not yet recruiting
Phase
Start date August 30, 2019
Completion date March 30, 2022

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