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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05111769
Other study ID # SEPSIS-HF
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date December 1, 2021
Est. completion date December 1, 2023

Study information

Verified date October 2021
Source Shanghai Zhongshan Hospital
Contact Minjie Ju, PHD
Phone 8613817014079
Email ju.minjie@zs-hospital.sh.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators intend to conduct clinical studies to determine the efficacy of rhBNP in the treatment of septic related dysfunction and kidney dysfunction


Description:

Sepsis is one of the common critical diseases in ICU with high mortality. Septic shock patients are often accompanied by multiple organ dysfunction (MODS), of which more than 50% of patients with varying degrees of myocardial injury.The investigators hope to find a drug with a protective effect on cardiac function and kidney function, so as to treat sepsis more effectively in the treatment of sepsis. Recombinant human brain natriuretic peptide (rhBNP) was approved by FDA in 2001 for the treatment of acute decompensated heart failure.These effects play a role in the protection of cardiac and kidney function, and have achieved good results in patients with cardiac insufficiency and AKI caused by cardiac surgery. The investigators are going to carry out related research from the following aspects: 1. To determine the effect of rhBNP on hemodynamics in sepsis based on PiCCO hemodynamic monitoring; 2. To collect and sort out the relevant data to determine the effects of rhBNP on cardiac function and kidney function, including cardiac ultrasound, kidney blood flow index and related laboratory tests. 3. To determine the effect of rhBNP on the final prognosis of patients, including ICU mortality and hospital mortality, ICU time, hospital stay, ventilator use time, kidney replacement therapy time, vasoactive drug dosage and time.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 70
Est. completion date December 1, 2023
Est. primary completion date December 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - sepsis complicated with heart failure(Diagnosed by sepsis 3.0) - Heart failure: BNP rises by 600 pg/ml - Age>=18 years old Exclusion Criteria: - Hemodynamically unstable - Pregnant - Disagree with comprehensive and active life support treatment - coronary heart disease, myocardial infarction, and cardiac insufficiency - chronic renal insufficiency

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Recombinant human brain natriuretic peptide
1. To determine the effect of rhBNP on hemodynamics in sepsis based on PiCCO hemodynamic monitoring; 2. To collect and sort out the relevant data to determine the effects of rhBNP on cardiac function and kidney function, including cardiac ultrasound, kidney blood flow index and related laboratory tests. 3. To determine the effect of rhBNP on the final prognosis of patients, including ICU mortality and hospital mortality, ICU time, hospital stay, ventilator use time, kidney replacement therapy time, vasoactive drug dosage and time.

Locations

Country Name City State
China Ju Minjie Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai Zhongshan Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary the effects of rhBNP(recombinant human brain natriuretic peptide) on cardiac function The decreasing trend of NTproBNP(N-terminal pro-B-type natriuretic peptide) 72 hours after rhBNP
Primary PiCCO hemodynamic monitoring in recombinant human brain natriuretic peptide group The improvement degree of cardiac index in recombinant human brain natriuretic peptide group 72 hours after recombinant human brain natriuretic peptide
Secondary ICU mortality and hospital mortality Comparison between rhBNP group and control group One month after entering ICU
Secondary Mechanical ventilation time after entering ICU Comparison between rhBNP group and control group 72 hours after recombinant human brain natriuretic peptide
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