Omics Sequencing of Exosomes in Body Fluids of Patients With Acute Lung Injury (NCT05058768) | Clinical Trial Compass
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Omics Sequencing of Exosomes in Body Fluids of Patients With Acute Lung Injury
China180 participantsStarted 2022-05-06
Plain-language summary
The exosomes in the experimental group and the control group were sequenced to find the difference of the two groups, providing a basis for subsequent basic research.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
Inclusion criteria of experimental group:
* Signed informed consent voluntarily;
* Age: \>18 years old, gender: no restrictions ;
* Patients with known clinical manifestations of respiratory impairment or new/aggravated respiratory symptoms diagnosed within one week of onset according to the Berlin definition guidelines.
Control group inclusion criteria:
* Age ≥18 years old (including 18 years old), male and female;
* Male weight ≥50 kg, female weight ≥45kg, and body mass index (BMI) between 19 and 26(inclusive), BMI= weight (kg)/ height (㎡);
* No smoking, alcohol addiction, no history of drug abuse;
* No diabetes, asthma, copd, chronic renal insufficiency and other basic diseases; No history of major diseases or infectious diseases (including hepatitis B, hepatitis C, HIV, syphilis);
* Those who have not taken drugs recently.
Exclusion Criteria:
Exclusion criteria of experimental group:
* Patients with diabetes, chronic renal insufficiency, malignant tumors and other basic diseases;
* severe malnutrition;
* Pregnant or lactating women;
* The researcher judged that he was not suitable to participate in this study.
Exclusion criteria for the control group:
* pregnant or lactation women;
* severe malnutrition;
* The researcher judged that he was not suitable to participate in this study.
What they're measuring
1
Compare the omics differences of blood samples between the experimental and control groups
Timeframe: one year
2
Compare the omics differences of urine samples between the experimental and control groups
Timeframe: one year
Trial details
NCT IDNCT05058768
SponsorNanfang Hospital, Southern Medical University