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Real Clinical Practice Register of AlbUminuRia Detection in Patients With Previously undiAgnosed Chronic Kidney Disease

Real Clinical Practice Register of AlbUminuRia Detection in Patients With Previously undiAgnosed Chronic Kidney Disease

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05690009
Acronym
AURA
Enrollment
4580
Registered
2023-01-19
Start date
2023-02-27
Completion date
2024-04-01
Last updated
2024-08-29

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

Conditions

Atrial Fibrillation, Cancer, Chronic Heart Failure, Chronic Kidney Diseases, Chronic Obstructive Pulmonary Disease, COVID-19, Hypertension, Ischemic Heart Disease, PreDiabetes, Urolithiasis

Keywords

Albumin-to-creatinine ratio, Albuminuria, Microalbuminuria, Chronic Kidney Diseases, Estimation of glomerular filtration rate

Brief summary

Real clinical practice register of Albuminuria detection in patients with previously undiagnosed chronic kidney disease

Detailed description

This register was sponsored and organized by the Association Eurasian Association of Internal Medicine. It is a multicenter non-interventional register of real clinical practice. The database will include patients aged 40 years and older without pre-existing nephrological disease who are available for a dipstick test for albuminuria. The subjects will be identified by screening all patients who meet inclusion/exclusion criteria during routine outpatient and hospital follow-up. The register does not include follow-up (cross-sectional design). Patients eligible for the register should be enrolled and documented. The procedure for obtaining informed consent for the collection and analysis of the retrospective data must comply with the local legislation. If necessary, patients will be asked to sign an informed consent document. All study sites will use standardized electronic CRFs. The Electronic Data Capture (EDC) system should be validated in accordance with current standards and legal requirements. The investigators will log into this system using individual usernames and passwords. Data may only be entered and corrected by the investigator or other authorized study site personnel.

Interventions

None listed

Sponsors

Eurasian Association of Therapists
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum

Inclusion criteria

* Men and women aged 40 and older at the time of data entry; * A possibility to check for albuminuria using dipsticks and/or analysis for microalbuminuria or albumin-to-creatinine ratio in a single urine sample.

Exclusion criteria

* Unwillingness of the patient to participate in the register; * Diagnosis of CKD made before the screening for the register; * Diagnosis of diabetes mellitus (DM) type 1 or type 2 made before the screening for the register; * Pregnancy; * Long distance running or very strenuous physical activity in the last 24 hours.

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of AU and its severity.Day 1Determination of AU by qualitative and/or quantitative methods

Secondary

MeasureTime frameDescription
Number of comorbidities per patient with AU.Day 1Number of comorbidities per patient with AU.
Frequency of prescribing renoprotective drugs.Day 1Frequency of prescribing renoprotective drugs.
Calculation of eGFR according to CKD-EPI formula 2021 in different phenotypes from the study population.Day 1Calculation of eGFR according to CKD-EPI formula 2021 in different phenotypes from the study population.
Prevalence of probable CKD in the study sample based on the clinical and laboratory data obtained during the screening.Day 1Prevalence of probable CKD in the study sample based on the clinical and laboratory data obtained during the screening.

Countries

Russia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026