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The value of changes in intestinal microbiome to the early diagnosis of sepsis-induced myocardial dysfunction

The value of changes in intestinal microbiome to the early diagnosis of sepsis-induced myocardial dysfunction

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800015709
Enrollment
Unknown
Registered
2018-04-16
Start date
2018-04-16
Completion date
Unknown
Last updated
2018-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

sepsis-induced myocardial dysfunction

Interventions

volunteers:no
septic patients with sepsis-induced myocardial dysfunction:no
septic patients without sepsis-induced myocardial dysfunction:no

Sponsors

Tongde Hospital of Zhejiang Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-85 years old men and women; 2. ICU in patients with sepsis (with Sepsis 3 APACHE, II = 8); 3. can do at least 28 days of research treatment; 4. has written informed consent signed by the Censorship Committee (IRB) / Independent Ethics Committee (IEC) and the privacy instructions specified by the state regulations.

Exclusion criteria

Exclusion criteria: 1. researchers judged the survival time of 25 score; 3. is known to have serious and clinically significant diseases (such as the New York Heart Association grading (NYHC) classification of IV grade congestive heart failure) or the inability to accept renal replacement therapy (such as hemofiltration, hemodialysis, or peritoneal dialysis); Severe renal dysfunction; 4. To be known to have chronic active hepatitis, alanine aminotransferase > 4 times the upper limit of normal value (ULN) and aspartate ammonia. Basal transferase > 4 * ULN, or total serum bilirubin >2 * ULN; 5. To be known to have a history of human immunodeficiency virus infection; 6. To be known to have abnormal amino acid metabolism, such as phenylketonuria, homocysteinuria or tyrosinemia; 7. had severe dyslipidemia, triglyceride level >2 * UN or >4.52mmol/L (>400mg/dL); 8. severe hyperglycemia, blood glucose >20mmol/L (>360mg/dL); 9. has clinically significant plasma electrolyte abnormalities, such as sodium ( 150mmol/L) and potassium (5.5mmol/L), calcium (3.0mmol/L) or phosphorus (1.62mmol/L); 10. To be known for pregnancy or lactation; On the first 30 days of L. recruitment, those who used antitumor chemotherapy drugs were treated with corticosteroids; 11. researchers believe that it is not suitable for any participant in the trial.

Design outcomes

Primary

MeasureTime frame
16S rDNA V3-V4 hypervariable regions of all bacteria in the stool samples;levels of D lactate;I-FABP, markers of inflammation and myocardial injury in the blood would be measured. T cell subsets would be sorted, and the expression of TLRs, NF-?B and PI3K / Akt in the blood;the activity of ureal ?-glucuronidase;

Countries

China

Contacts

Public ContactJianbiao Meng

Tongde Hospital of Zhejiang Province

mjb1050@163.com+86 13486115715

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 14, 2026