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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03282409
Other study ID # AOR16089
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date April 26, 2018
Est. completion date February 2025

Study information

Verified date September 2023
Source Assistance Publique - Hôpitaux de Paris
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study aims to develop and validate a prediction score of chronic renal disease occurrence within 3 years after ICU discharge in patients who suffered an acute kidney failure during ICU stay and recovered normal renal function at 90 days following their discharge. The primary study outcome is the incidence of chronic renal disease within the first 3 years after ICU discharge, defined by a lower glomerular filtration rate (GFR) under 60 mL/minute/1.73m2.


Description:

As second objectives, the study aims to: - Evaluate the GFR decline in patients who had an underlying chronic kidney disease. - Evaluate factors associated with a persistent decreased GFR at day-90. - Characterization the clinical and biological phenotype of chronic renal disease in these patients. - Evaluate treatments provided to these patients according to CKD occurence. - Evaluate the rate of cardiovascular and thrombo-embolic morbidity-mortality. - Assess the quality of life every year for 3 years. - Evaluate the medico-economic burden of CKD.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 425
Est. completion date February 2025
Est. primary completion date February 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient ? 18 years; - Patient suffering an acute kidney injury (defined by AKIN score ?1) during ICU stay; - Patient discharged alive from the ICU; - Patient's signed consent obtained; - Patient covered by a healthcare insurance. Exclusion Criteria: - Pregnant or breastfeeding woman; - SOFA score < 1 (except for kidney assessment) at time of ICU admission; - End-stage of renal failure or dialysis treatment or renal transplantation prior to ICU admission; - Patient treated with dialysis at ICU discharge; - Immunosuppressive treatment prior to ICU admission; - Patient under legal incapacity (tutor or guardian protection); - Being unable to follow-up of the study; - Life expectancy expected shorter than 90 days; - Refusal to participate in the study; - Patient's main address is outside of Il de France region for the centers in this region; - Patient < 18 years; - Patient not affiliated to national social security scheme; - Patient deprived of liberty by judicial measure.

Study Design


Locations

Country Name City State
France Intensive care unit, Ambroise Pare Hospital Boulogne Billancourt Hauts-de-seine

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of chronic kidney disease Incidence of chronic kidney disease defined by a decreased glomerular filtration rate (GFR) under 60 mL/minute/1.73m2. At 3 years
Secondary Progression of chronic renal disease defined by the slope of GFR decline For patients who have chronic renal disease history and developped an acute kidney failure during ICU stay, progression of chronic renal disease defined by a GFR decline greater than 30% at 3 years. At 3 years
Secondary Progression of the proteinuria Evolution of urinary protein to creatinine ratio (mg/mmol). At 3 years
Secondary Progression of chronic renal disease defined by the number of patients with end-stage renal disease requiring dialysis or renal transplantation For patients who have chronic renal disease history and developped an acute kidney failure during ICU stay, progression of chronic renal disease defined by need to dialysis, or need a renal transplantation, and GFR < 15mL/minute/1.73m2. At 3 years
Secondary Occurrence of cardiovascular events and thromboembolic events Cardiovascular events include acute coronary syndrome, ischemic stroke, peripheral artery disease, ventricular rhythm disorder and sudden death.
Thromboembolic events included deep vein thrombosis and pulmonary embolism.
At 3 years
Secondary All-cause mortality All-cause mortality and cardiovascular cause mortality At 3 years
Secondary Quality of life assessment Assessment of quality of life of patients by the scale KDQOL-SF-12. The SF-12 is a short form that includes Items 1-12 as generic core of kidney Disease Quality of Life Instrument (KDQOL). At the end of 1 year
Secondary Quality of life assessment Assessment of quality of life of patients by the scale EQ-5D-5L. The EQ-5D-5L questionnaire consists the descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state. At the end of 1 year
Secondary Cost Costs related to medical care At 3 years
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