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The Effect of rTEM in the Prognosis and Severity of Sepsis Induced ARDS

S

Southeast University, China

Status

Not yet enrolling

Conditions

Sepsis

Treatments

Other: Taking peripheral blood

Study type

Observational

Funder types

Other

Identifiers

NCT06063707
2022ZDSYLL402-P01

Details and patient eligibility

About

To observe the changes of plasma rTEM levels in patients with sepsis, sepsis induced ARDS, and to explore its clinical significance.

Full description

90 patients will be included in this study. Blood samples from these patients in the first day, the third day, were maintained and tested to detect the change of rTEM level. Severity of illness and survival status of every patient were recorded within 28 days. The objective is to observe the changes of plasma rTEM levels in patients with sepsis, sepsis induced ARDS, and to explore its clinical significance.

Enrollment

90 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Diagnosed as Sepsis 3.0 Patients signing informed consent

Exclusion criteria

Pregnant women Patients with tumor、hepatitis、liver cirrhosis、acute myocardial infarction、chronic renal tubular nephritis、interstitial pneumonia、acute pancreatitis、systemic lupus erythenatosus、ulcerative colitis、crohn's disease、HELLP syndrome

Trial design

90 participants in 2 patient groups

Survivors
Description:
Sepsis induced ARDS patients who survived
Treatment:
Other: Taking peripheral blood
Nonsurvivors
Description:
Sepsis induced ARDS patients who not survived
Treatment:
Other: Taking peripheral blood

Trial contacts and locations

0

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Central trial contact

Jingyuan Xu, M.D.

Data sourced from clinicaltrials.gov

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