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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05597332
Other study ID # 61447422.1.1001.5404
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date November 2022
Est. completion date July 2023

Study information

Verified date November 2022
Source University of Campinas, Brazil
Contact Lygia Lussim
Phone +55 19 3521-7362
Email lylussim@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical interventional study is to learn about the effect of implementing a care bundle in the progression of acute kidney injury (AKI) in critical patients. The main questions it aims to answer are: - What is the impact of care bundle in AKI progression? - Some improvement of care bundle adhesion rate through an electronic alert can be achieved? Participants will be adults and critical patients with AKI. During observational study the incidence and progression of AKI will be measured, as well spontaneous care bundle adhesion by medical team. In the interventional study, the progression rate of AKI influenced by care bundle will be measured, as well the adhesion of care bundle through an electronic alert inserted in the patient's daily medical record.


Description:

This is a clinical, multicentric and prospective trial (study type: "before" and "after"). Patients aged ≥18 years, admitted to clinical and surgical intensive care units (ICUs) will be included according to selection criteria. During observational and interventional studies clinical and laboratorial information from electronic medical records will be registered. AKI diagnosis and classification will be based on serum creatinine levels according to kidney disease improving global outcomes (KDIGO) criteria. The observational study will be carried out to measure the incidence of AKI KDIGO 1 and its progression rate, in order to estimate sample size for the interventional study. Researchers assumed a 10% to 20% reduction in the progression of AKI KDIGO 1 to more advanced stages after the implementation of the care bundle. In the interventional study, the care bundle will be included in the medical records of each individual who develops AKI KDIGO 1. Patients included in this study will be followed by 7 days from inclusion. Adhesion rate to the care bundle will be measured between observational and interventional studies.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 400
Est. completion date July 2023
Est. primary completion date March 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients with recent ICU admission (= 48 hours) - Patients without AKI or with AKI KDIGO 1 at the time of admission Exclusion Criteria: - Patients with chronic kidney disease, stage 4 to 5D - Patients with kidney transplant - Patients with AKI KDIGO 2, 3 or on dialysis at the time of inclusion in the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Care bundle for AKI
To maintain mean arterial pressure (MAP) = 65 mmHg; to keep the patient euvolemic; to avoid nephrotoxic drugs; to adjust dose of medication for kidney function; to exclude urinary obstruction; to monitor urine output and serum creatinine levels.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
University of Campinas, Brazil Universidade Estadual Paulista Júlio de Mesquita Filho

Outcome

Type Measure Description Time frame Safety issue
Primary AKI progression AKI progression from KDIGO 1 to KDIGO 2 or 3 = 7 days from inclusion
Secondary Adherence to care bundle Adhesion rate associated to AKI-care bundle = 7 days from inclusion
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