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NCT06156098 Clinical Trial

Bedside Renal Ultrasound Assessment in Patients With Acute Kidney Injury

Critical Illness Clinical Trial

Official title:
Bedside Renal Ultrasound Assessment in Critically Ill Patients With Acute Kidney Injury: an Observational Study

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06156098
Other study ID # TJ-IRB202308105
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 1, 2023
Est. completion date September 30, 2024

Study information
Verified date April 2024
Source Tongji Hospital
Contact Xiao Zhang, phd
Phone 15926207366
Email ranxiao1001@tjh.tjmu.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Exploring the predictive and evaluative value of various indicators of bedside critical renal ultrasound in critically ill patients with acute kidney injury (AKI)

Description:

This study aims to perform bedside renal ultrasound examinations on critically ill patients admitted to the ICU (including sepsis, respiratory failure, shock, multiple trauma, etc.) and prospectively observe the relationship between ultrasound parameters and the occurrence and progression of AKI, in conjunction with traditional renal function indicators. This will provide clinicians with a rapid, non-invasive, and visual examination tool at the bedside for early diagnosis and treatment of AKI.

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date September 30, 2024
Est. primary completion date November 30, 2023
Accepts healthy volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Age = 18 years and = 70 years - Criteria for sepsis patients Exclusion Criteria: - Pregnant women. - Patients with malignant tumors, severe heart failure, chronic renal insufficiency, end stage renal disease, kidney transplantation.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• No Intervention
No Intervention

Locations
Country Name City State
China Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan Hubei

Sponsors (1)
Lead Sponsor Collaborator
Qin Zhang

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Survival 28-day mortality rate 28 days
Secondary AKI duration of continuous renal replacement therapy (CRRT)during hospitalization, length of hospital stay, duration of ICU stay, hospital mortality rate, 28-day mortality rate, and other relevant data. 28 days
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